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 |
Related structures:
AlphaFold database: A4HPJ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0016192 | vesicle-mediated transport | 4 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.648 |
CLV_MEL_PAP_1 | 61 | 67 | PF00089 | 0.296 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.390 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.502 |
CLV_Separin_Metazoa | 244 | 248 | PF03568 | 0.587 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.606 |
DOC_ANK_TNKS_1 | 435 | 442 | PF00023 | 0.597 |
DOC_CDC14_PxL_1 | 278 | 286 | PF14671 | 0.435 |
DOC_CYCLIN_RxL_1 | 369 | 378 | PF00134 | 0.525 |
DOC_MAPK_FxFP_2 | 37 | 40 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 27 | 37 | PF00069 | 0.239 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.418 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.500 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 307 | 310 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.620 |
DOC_PP2B_LxvP_1 | 513 | 516 | PF13499 | 0.734 |
DOC_PP4_FxxP_1 | 222 | 225 | PF00568 | 0.648 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.526 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.421 |
DOC_SPAK_OSR1_1 | 64 | 68 | PF12202 | 0.296 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.324 |
DOC_USP7_UBL2_3 | 406 | 410 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.324 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 480 | 489 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 76 | 85 | PF00244 | 0.364 |
LIG_Actin_WH2_2 | 422 | 438 | PF00022 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 467 | 476 | PF00928 | 0.519 |
LIG_EH1_1 | 505 | 513 | PF00400 | 0.502 |
LIG_eIF4E_1 | 506 | 512 | PF01652 | 0.602 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.334 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.321 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.559 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.574 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.525 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.664 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.527 |
LIG_GBD_Chelix_1 | 297 | 305 | PF00786 | 0.553 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.707 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.522 |
LIG_NRBOX | 116 | 122 | PF00104 | 0.324 |
LIG_REV1ctd_RIR_1 | 172 | 181 | PF16727 | 0.404 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 257 | 261 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 319 | 322 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 506 | 509 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.495 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.230 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 484 | 490 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 128 | 134 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 336 | 343 | PF11976 | 0.439 |
LIG_TYR_ITIM | 301 | 306 | PF00017 | 0.546 |
LIG_WRC_WIRS_1 | 171 | 176 | PF05994 | 0.404 |
MOD_CDK_SPxK_1 | 430 | 436 | PF00069 | 0.622 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.615 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.640 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.371 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.465 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.521 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.533 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.543 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.471 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.393 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.630 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.531 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.621 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.421 |
MOD_CMANNOS | 469 | 472 | PF00535 | 0.540 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.572 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.586 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.423 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.683 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.585 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.410 |
MOD_GlcNHglycan | 345 | 350 | PF01048 | 0.473 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.499 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.552 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.676 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.324 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.586 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.621 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.463 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.532 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.579 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.544 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.239 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.473 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.610 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.536 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.342 |
MOD_N-GLC_1 | 482 | 487 | PF02516 | 0.457 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.696 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.183 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.574 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.520 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.471 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.445 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.338 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.502 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.607 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.429 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.239 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.371 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.493 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.502 |
MOD_Plk_1 | 482 | 488 | PF00069 | 0.489 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.490 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.496 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.508 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.446 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.649 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.536 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.600 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.589 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.527 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.482 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.627 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.324 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.526 |
TRG_DiLeu_LyEn_5 | 507 | 512 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 404 | 407 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 502 | 507 | PF00026 | 0.601 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HW11 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IR86 | Leishmania donovani | 77% | 100% |
A4ID71 | Leishmania infantum | 77% | 100% |
E9ATA4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q193 | Leishmania major | 76% | 100% |