A small protein family largely unrelated to amastins.. Only expanded mildly during evolution compared to amastins
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: 0 |
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 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: A0A3S5H7A1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 408 | 414 | PF00089 | 0.477 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.626 |
DEG_APCC_DBOX_1 | 432 | 440 | PF00400 | 0.690 |
DEG_SPOP_SBC_1 | 330 | 334 | PF00917 | 0.757 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.690 |
DOC_CKS1_1 | 355 | 360 | PF01111 | 0.644 |
DOC_CKS1_1 | 381 | 386 | PF01111 | 0.693 |
DOC_CYCLIN_yClb1_LxF_4 | 123 | 128 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.382 |
DOC_MAPK_gen_1 | 223 | 231 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 223 | 231 | PF00069 | 0.592 |
DOC_PP1_RVXF_1 | 123 | 129 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 347 | 350 | PF13499 | 0.710 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.703 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.391 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.767 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.691 |
LIG_14-3-3_CanoR_1 | 183 | 190 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 279 | 284 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 336 | 345 | PF00244 | 0.836 |
LIG_Actin_WH2_2 | 448 | 463 | PF00022 | 0.672 |
LIG_APCC_ABBA_1 | 193 | 198 | PF00400 | 0.357 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.349 |
LIG_deltaCOP1_diTrp_1 | 19 | 28 | PF00928 | 0.582 |
LIG_EVH1_2 | 352 | 356 | PF00568 | 0.664 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.443 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.551 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.327 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.242 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.345 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.275 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.550 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.694 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.715 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.369 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.554 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.321 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.654 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.704 |
LIG_GBD_Chelix_1 | 30 | 38 | PF00786 | 0.312 |
LIG_LIR_Gen_1 | 134 | 142 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 27 | 35 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 388 | 398 | PF02991 | 0.801 |
LIG_LIR_Gen_1 | 466 | 473 | PF02991 | 0.689 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.800 |
LIG_LIR_Nem_3 | 466 | 470 | PF02991 | 0.690 |
LIG_PCNA_yPIPBox_3 | 169 | 183 | PF02747 | 0.377 |
LIG_PDZ_Class_2 | 539 | 544 | PF00595 | 0.723 |
LIG_PTB_Apo_2 | 103 | 110 | PF02174 | 0.312 |
LIG_PTB_Apo_2 | 210 | 217 | PF02174 | 0.312 |
LIG_PTB_Apo_2 | 51 | 58 | PF02174 | 0.334 |
LIG_PTB_Apo_2 | 83 | 90 | PF02174 | 0.366 |
LIG_PTB_Phospho_1 | 103 | 109 | PF10480 | 0.312 |
LIG_PTB_Phospho_1 | 83 | 89 | PF10480 | 0.372 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.550 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.375 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.689 |
LIG_SH2_NCK_1 | 190 | 194 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.754 |
LIG_SH2_NCK_1 | 467 | 471 | PF00017 | 0.689 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.376 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 196 | 200 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.322 |
LIG_SH3_2 | 358 | 363 | PF14604 | 0.655 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.733 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.652 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.741 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.766 |
LIG_SH3_3 | 500 | 506 | PF00018 | 0.715 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 151 | 156 | PF11976 | 0.388 |
LIG_SUMO_SIM_anti_2 | 27 | 33 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 151 | 158 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 202 | 208 | PF11976 | 0.310 |
LIG_TYR_ITIM | 135 | 140 | PF00017 | 0.551 |
LIG_WRC_WIRS_1 | 156 | 161 | PF05994 | 0.310 |
MOD_CDK_SPxxK_3 | 13 | 20 | PF00069 | 0.622 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.637 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.665 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.696 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.711 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.368 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.558 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.488 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.760 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.654 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.779 |
MOD_DYRK1A_RPxSP_1 | 380 | 384 | PF00069 | 0.692 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.388 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.632 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.279 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.471 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.495 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.595 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.519 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.532 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.314 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.329 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.297 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.651 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.674 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.714 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.697 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.340 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.711 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.707 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.552 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.383 |
MOD_N-GLC_1 | 456 | 461 | PF02516 | 0.440 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.530 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.308 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.423 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.262 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.353 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.642 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.637 |
MOD_PKA_1 | 336 | 342 | PF00069 | 0.760 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.362 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.650 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.685 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.698 |
MOD_PKB_1 | 336 | 344 | PF00069 | 0.761 |
MOD_PKB_1 | 481 | 489 | PF00069 | 0.728 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.688 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.705 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.340 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.371 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.455 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.559 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.441 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.688 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.298 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.699 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.693 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.666 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.694 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.680 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 339 | 347 | PF00179 | 0.812 |
MOD_SUMO_rev_2 | 452 | 458 | PF00179 | 0.674 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.754 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.690 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.734 |
TRG_NES_CRM1_1 | 151 | 167 | PF08389 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA63 | Leptomonas seymouri | 52% | 94% |
A4HC03 | Leishmania braziliensis | 66% | 94% |
A4HZG0 | Leishmania infantum | 99% | 100% |
E9AVE0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QC39 | Leishmania major | 88% | 97% |