Publication identifier(s): 8702946
A surface coat protein involved in immune evasion in Leishmaniids. Extremely fast evolving, almost completely disordered mucin-like protein. . Localization: Cell surface (experimental)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 65 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 39, no: 7 |
NetGPI | no | yes: 0, no: 46 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 47 |
GO:0042995 | cell projection | 2 | 47 |
GO:0043226 | organelle | 2 | 47 |
GO:0043227 | membrane-bounded organelle | 3 | 47 |
GO:0110165 | cellular anatomical entity | 1 | 47 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 47 |
GO:0016020 | membrane | 2 | 7 |
Related structures:
AlphaFold database: A4HJC8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.319 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.484 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.427 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.674 |
DOC_CYCLIN_yCln2_LP_2 | 243 | 249 | PF00134 | 0.229 |
DOC_MAPK_gen_1 | 13 | 20 | PF00069 | 0.672 |
DOC_MAPK_gen_1 | 278 | 286 | PF00069 | 0.508 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.633 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.262 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.532 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.456 |
LIG_14-3-3_CanoR_1 | 110 | 118 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.472 |
LIG_APCC_ABBA_1 | 85 | 90 | PF00400 | 0.293 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.211 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.218 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 68 | 72 | PF00533 | 0.326 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.333 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.376 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.642 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.436 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.463 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.409 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.477 |
LIG_KLC1_Yacidic_2 | 86 | 90 | PF13176 | 0.275 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 186 | 195 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 225 | 233 | PF02991 | 0.255 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.495 |
LIG_NRBOX | 24 | 30 | PF00104 | 0.604 |
LIG_Pex14_1 | 163 | 167 | PF04695 | 0.263 |
LIG_Pex14_2 | 53 | 57 | PF04695 | 0.298 |
LIG_SH2_GRB2like | 143 | 146 | PF00017 | 0.470 |
LIG_SH2_GRB2like | 167 | 170 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 42 | 46 | PF00017 | 0.319 |
LIG_SH2_PTP2 | 139 | 142 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 167 | 171 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 167 | 170 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.583 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.413 |
LIG_SUMO_SIM_anti_2 | 207 | 213 | PF11976 | 0.221 |
LIG_TRFH_1 | 27 | 31 | PF08558 | 0.361 |
LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.410 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.339 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.317 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.310 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.428 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.463 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.488 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.361 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.429 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.484 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.383 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.284 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.301 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.510 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.435 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.719 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.473 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.411 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.371 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.327 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.406 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.428 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.546 |
MOD_LATS_1 | 108 | 114 | PF00433 | 0.188 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.526 |
MOD_N-GLC_2 | 299 | 301 | PF02516 | 0.512 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.418 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.362 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.320 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.482 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.321 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.328 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.311 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.248 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.484 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.391 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.310 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.577 |
MOD_PK_1 | 110 | 116 | PF00069 | 0.229 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.374 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.441 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.537 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.405 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.476 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.345 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.381 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.379 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.458 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P227 | Leptomonas seymouri | 33% | 96% |
A0A0N0P276 | Leptomonas seymouri | 30% | 98% |
A0A0N0P2E6 | Leptomonas seymouri | 28% | 100% |
A0A0N0P2L4 | Leptomonas seymouri | 33% | 100% |
A0A0N0P4M2 | Leptomonas seymouri | 26% | 100% |
A0A0N1HY53 | Leptomonas seymouri | 38% | 100% |
A0A0S4IN83 | Bodo saltans | 30% | 100% |
A0A0S4IR61 | Bodo saltans | 29% | 75% |
A0A0S4IVH1 | Bodo saltans | 31% | 100% |
A0A0S4IVI8 | Bodo saltans | 24% | 100% |
A0A0S4IZC7 | Bodo saltans | 30% | 73% |
A0A0S4J2R4 | Bodo saltans | 24% | 90% |
A0A0S4J353 | Bodo saltans | 27% | 100% |
A0A0S4J3T7 | Bodo saltans | 31% | 67% |
A0A0S4J805 | Bodo saltans | 30% | 100% |
A0A0S4JCG7 | Bodo saltans | 32% | 80% |
A0A0S4JEK1 | Bodo saltans | 26% | 74% |
A0A0S4JEZ2 | Bodo saltans | 30% | 95% |
A0A0S4JMG0 | Bodo saltans | 25% | 87% |
A0A0S4JS12 | Bodo saltans | 26% | 67% |
A0A0S4JSH3 | Bodo saltans | 31% | 85% |
A0A0S4JU20 | Bodo saltans | 28% | 100% |
A0A0S4KHE4 | Bodo saltans | 31% | 82% |
A0A0S4KL26 | Bodo saltans | 28% | 83% |
A0A1X0NKN8 | Trypanosomatidae | 27% | 100% |
A0A3Q8I9A6 | Leishmania donovani | 32% | 78% |
A0A3Q8I9D0 | Leishmania donovani | 34% | 100% |
A0A3Q8IFC2 | Leishmania donovani | 32% | 69% |
A0A3Q8IIJ9 | Leishmania donovani | 69% | 100% |
A0A3S5H6D6 | Leishmania donovani | 24% | 100% |
A0A3S7WPB2 | Leishmania donovani | 21% | 100% |
A0A3S7X4J4 | Leishmania donovani | 69% | 100% |
A4H4G6 | Leishmania braziliensis | 23% | 100% |
A4H5P0 | Leishmania braziliensis | 25% | 100% |
A4HBX3 | Leishmania braziliensis | 35% | 67% |
A4HJX1 | Leishmania braziliensis | 35% | 69% |
A4HTX9 | Leishmania infantum | 24% | 100% |
A4HVB0 | Leishmania infantum | 31% | 75% |
A4I6S2 | Leishmania infantum | 30% | 69% |
A4I6S4 | Leishmania infantum | 69% | 100% |
A7PW81 | Vitis vinifera | 28% | 91% |
E8NHG5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 68% |
E8NHP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9AG65 | Leishmania infantum | 21% | 100% |
E9AGG5 | Leishmania infantum | 34% | 72% |
E9AGH0 | Leishmania infantum | 34% | 80% |
E9AKM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9AMQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AP02 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 89% |
E9AP03 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 77% |
E9AP07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 82% |
E9AP08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 72% |
E9B1U3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 66% |
E9B1U4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 88% |
E9B1U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 72% |
E9B1U6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
P35334 | Phaseolus vulgaris | 24% | 88% |
P58822 | Phaseolus vulgaris | 24% | 88% |
P58823 | Phaseolus vulgaris | 24% | 88% |
Q25331 | Leishmania major | 30% | 100% |
Q4Q6B6 | Leishmania major | 69% | 100% |
Q4Q6B7 | Leishmania major | 69% | 100% |
Q4QC79 | Leishmania major | 36% | 66% |
Q4QGJ4 | Leishmania major | 30% | 100% |
Q4QGJ7 | Leishmania major | 30% | 100% |
Q4QGK6 | Leishmania major | 30% | 100% |
Q4QGL4 | Leishmania major | 32% | 100% |
Q4QHW6 | Leishmania major | 26% | 100% |
Q8GT95 | Oryza sativa subsp. japonica | 28% | 91% |
Q9LH52 | Arabidopsis thaliana | 28% | 93% |
Q9M5J8 | Arabidopsis thaliana | 24% | 92% |
Q9M5J9 | Arabidopsis thaliana | 24% | 92% |