mutLBSgeneDB

mutLBSgeneDB
mutated Ligand Binding Site gene DataBase

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Gene Summary

Ligand Binding Site Mutation Information

Protein Structure Related Information

Gene Expression and Gene-Gene Network

Phenotype Information

Pharmacological Information

Conservation Information for LBS

Gene summary for HSP90B1
Gene summary
Basic gene Info.Gene symbolHSP90B1
Gene nameheat shock protein 90kDa beta (Grp94), member 1
SynonymsECGP|GP96|GRP94|HEL-S-125m|HEL35|TRA1
CytomapUCSC genome browser: 12q24.2-q24.3
Type of geneprotein-coding
RefGenesNM_003299.2,
Description94 kDa glucose-regulated proteinendoplasminendothelial cell (HBMEC) glycoproteinepididymis luminal protein 35epididymis secretory sperm binding protein Li 125mheat shock protein 90 kDa beta member 1stress-inducible tumor rejection antigen gp96tumor
Modification date20141207
dbXrefs MIM : 191175
HGNC : HGNC
Ensembl : ENSG00000166598
HPRD : 01860
Vega : OTTHUMG00000170118
ProteinUniProt: P14625
go to UniProt's Cross Reference DB Table
ExpressionCleanEX: HS_HSP90B1
BioGPS: 7184
PathwayNCI Pathway Interaction Database: HSP90B1
KEGG: HSP90B1
REACTOME: HSP90B1
Pathway Commons: HSP90B1
ContextiHOP: HSP90B1
ligand binding site mutation search in PubMed: HSP90B1
UCL Cancer Institute: HSP90B1
Assigned class in mutLBSgeneDBC: This gene just belongs to mutLBSgenes.

Gene ontology having evidence of Inferred from Direct Assay (IDA) from Entrez
GO IDGO TermPubMed ID
GO:0001666response to hypoxia15620698
GO:0031247actin rod assembly19000834
GO:0043666regulation of phosphoprotein phosphatase activity19000834
GO:0071318cellular response to ATP19000834


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Ligand binding site mutations for HSP90B1

Cancer type specific mutLBS sorted by frequency
LBSAAchange of nsSNVCancer type# samples
A111D113ECOAD1
Y200Y200FCOAD1
W223E224KUCEC1
cf) Cancer type abbreviation. BLCA: Bladder urothelial carcinoma, BRCA: Breast invasive carcinoma, CESC: Cervical squamous cell carcinoma and endocervical adenocarcinoma, COAD: Colon adenocarcinoma, GBM: Glioblastoma multiforme, LGG: Brain lower grade glioma, HNSC: Head and neck squamous cell carcinoma, KICH: Kidney chromophobe, KIRC: Kidney renal clear cell carcinoma, KIRP: Kidney renal papillary cell carcinoma, LAML: Acute myeloid leukemia, LUAD: Lung adenocarcinoma, LUSC: Lung squamous cell carcinoma, OV: Ovarian serous cystadenocarcinoma, PAAD: Pancreatic adenocarcinoma, PRAD: Prostate adenocarcinoma, SKCM: Skin cutaneous melanoma, STAD: Stomach adenocarcinoma, THCA: Thyroid carcinoma, UCEC: Uterine corpus endometrial carcinoma.


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Protein structure related information for HSP90B1
Relative protein structure stability change (ΔΔE) using Mupro 1.1
Mupro score denotes assessment of the effect of mutations on thermodynamic stability.
  (ΔΔE<0: mutation decreases stability, ΔΔE>0: mutation increases stability)
: nsSNV at non-LBS: nsSNV at LBS

nsSNVs sorted by the relative stability change of protein structure by each mutation
Blue: mutations of positive stability change. and red : the most recurrent mutation for this gene.
LBSAAchange of nsSNVRelative stability change
W223E224K-1.0030538
Y200Y200F-0.46905518
A111D113E-0.34353756
(MuPro1.1: Jianlin Cheng et al., Prediction of Protein Stability Changes for Single-Site Mutations Using Support Vector Machines, PROTEINS: Structure, Function, and Bioinformatics. 2006, 62:1125-1132)

Structure image for HSP90B1 from PDB

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Differential gene expression and gene-gene network for HSP90B1
Differential gene expression between mutated and non-mutated LBS samples in all 16 major cancer types

Differential co-expressed gene network based on protein-protein interaction data (CePIN)
* Left PPI network was created from samples with mutations in the LBS of HSP90B1 and the right PPI network was created from samples without mutations in the LBS of HSP90B1. Only genes with p-value < 0.05 are shown.
Red circle: input gene. Orange circle: LBSgene. Blue circle: other gene.


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Phenotype information for HSP90B1
Gene level disease information (DisGeNet)
Disease IDDisease name# PubMedAssociation type
umls:C0033578Prostatic Neoplasms2Biomarker

Mutation level pathogenic information (ClinVar annotation)
Allele IDAA changeClinical significanceOriginPhenotype IDs

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Pharmacological information for HSP90B1
Gene expression profile of anticancer drug treated cell-lines (CCLE)
Heatmap showing the correlation between gene expression and drug response across all the cell-lines. We chose the top 20 among 138 drugs.We used Pearson's correlation coefficient.

Gene-centered drug-gene interaction network
Drug information targeting mutLBSgene (Approved drugs only)
Drug statusDrugBank IDNameTypeDrug structure
ApprovedDB00615RifabutinSmall molecule
ExperimentalDB021032-ChlorodideoxyadenosineSmall molecule
ExperimentalDB029351-Methoxy-2-(2-Methoxyethoxy)EthaneSmall molecule
ExperimentalDB03719N-Ethyl-5'-Carboxamido AdenosineSmall molecule
ExperimentalDB03758RadicicolSmall molecule
ExperimentalDB08464METHYL 3-CHLORO-2-{3-[(2,5-DIHYDROXY-4-METHOXYPHENYL)AMINO]-3-OXOPROPYL}-4,6-DIHYDROXYBENZOATESmall molecule
ExperimentalDB084652-(3-AMINO-2,5,6-TRIMETHOXYPHENYL)ETHYL 5-CHLORO-2,4-DIHYDROXYBENZOATESmall molecule

Gene-centered ligand-gene interaction network

Ligands binding to mutated ligand binding site of HSP90B1 go to BioLip
Ligand IDLigand short nameLigand long namePDB IDPDB namemutLBS
2LC2-FLUORO-6-[(3S)-TETRAHYDROFURAN-3-YLAMINO]-4-(3,6,6- TRIMETHYL-4-OXO-4,5,6,7-TETRAHYDRO-1H-INDOL-1-YL) BENZAMIDE4nh9AA111 Y200 W223


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Conservation information for LBS of HSP90B1
Multiple alignments for P14625 in multiple species
LBSAA sequence# speciesSpecies
A108ELISNASDALD7Homo sapiens, Caenorhabditis elegans, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
A111SNASDALDKIR7Homo sapiens, Caenorhabditis elegans, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
D149LLHVTDTGVGM5Homo sapiens, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
D149LLHITDTGVGM1Caenorhabditis elegans
D149MLHVTDTGIGM1Gallus gallus
E158GMTREELVKNL5Homo sapiens, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
E158GMTRQDLINNL1Caenorhabditis elegans
E158GMTKEELIKNL1Gallus gallus
F199QFGVGFYSAFL6Homo sapiens, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
F199QFGVGFYAAFL1Caenorhabditis elegans
I247GRGTTITLVLK6Homo sapiens, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
I247KRGTQITLYLK1Caenorhabditis elegans
M154DTGVGMTREEL5Homo sapiens, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
M154DTGVGMTRQDL1Caenorhabditis elegans
M154DTGIGMTKEEL1Gallus gallus
N107RELISNASDAL7Homo sapiens, Caenorhabditis elegans, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
T245TLGRGTTITLV6Homo sapiens, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
T245TLKRGTQITLY1Caenorhabditis elegans
V211ADKVIVTSKHN5Homo sapiens, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
V211ADRVVVTTKNN1Caenorhabditis elegans
V211ADRVIVTSKHN1Gallus gallus
W223DTQHIWESDSN6Homo sapiens, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
W223DDQYIWESDSA1Caenorhabditis elegans
Y200FGVGFYSAFLV6Homo sapiens, Gallus gallus, Mus musculus, Rattus norvegicus, Canis lupus familiaris, Bos taurus
Y200FGVGFYAAFLV1Caenorhabditis elegans


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