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Accession Number: | P51811 |
Protein Name: | MEMBRANE TRANSPORT PROTEIN XK (KX ANTIGEN) - Homo sapiens (Human). |
Length: | 444 |
Molecular Weight: | 50902.00 |
Species: | Homo sapiens (Human) [9606] |
Number of TMSs: | 9 |
Location1 / Topology2 / Orientation3: | Membrane1 / Multi-pass membrane protein2 |
Substrate | alpha-amino acid |
Cross database links:
RefSeq: | NP_066569.1 |
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Entrez Gene ID: | 7504 |
Pfam: | PF09815 |
OMIM: |
314850 gene+phenotype |
KEGG: | hsa:7504 |
Gene Ontology
GO:0016021
C:integral to membrane
GO:0005515
F:protein binding
GO:0005215
F:transporter activity
GO:0006865
P:amino acid transport
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References (8)[1] “Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.” Ho M.et.al. 8004674 [2] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [3] “Purification and partial characterization of the erythrocyte Kx protein deficient in McLeod patients.” Khamlichi S.et.al. 7737196 |
External Searches:
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Analyze:
Predict TMSs (Predict number of transmembrane segments) | ||||
FASTA formatted sequence |
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1: MKFPASVLAS VFLFVAETTA ALSLSSTYRS GGDRMWQALT LLFSLLPCAL VQLTLLFVHR 61: DLSRDRPLVL LLHLLQLGPL FRCFEVFCIY FQSGNNEEPY VSITKKRQMP KNGLSEEIEK 121: EVGQAEGKLI THRSAFSRAS VIQAFLGSAP QLTLQLYISV MQQDVTVGRS LLMTISLLSI 181: VYGALRCNIL AIKIKYDEYE VKVKPLAYVC IFLWRSFEIA TRVVVLVLFT SVLKTWVVVI 241: ILINFFSFFL YPWILFWCSG SPFPENIEKA LSRVGTTIVL CFLTLLYTGI NMFCWSAVQL 301: KIDSPDLISK SHNWYQLLVY YMIRFIENAI LLLLWYLFKT DIYMYVCAPL LVLQLLIGYC 361: TAILFMLVFY QFFHPCKKLF SSSVSEGFQR WLRCFCWACR QQKPCEPIGK EDLQSSRDRD 421: ETPSSSKTSP EPGQFLNAED LCSA