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. | yes | yes: 20 |
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: 3, no: 6 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF83
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.541 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.535 |
CLV_PCSK_PC7_1 | 3 | 9 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.766 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.721 |
DEG_APCC_DBOX_1 | 299 | 307 | PF00400 | 0.516 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.576 |
DEG_COP1_1 | 250 | 259 | PF00400 | 0.582 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.790 |
DEG_ODPH_VHL_1 | 11 | 22 | PF01847 | 0.426 |
DOC_MAPK_DCC_7 | 255 | 265 | PF00069 | 0.537 |
DOC_MAPK_DCC_7 | 7 | 16 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 337 | 343 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 7 | 16 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 10 | 18 | PF00069 | 0.629 |
DOC_PP1_RVXF_1 | 306 | 312 | PF00149 | 0.493 |
DOC_PP4_FxxP_1 | 228 | 231 | PF00568 | 0.564 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.456 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.543 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 484 | 489 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 141 | 146 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 285 | 294 | PF00244 | 0.582 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 557 | 567 | PF00244 | 0.493 |
LIG_14-3-3_CterR_2 | 569 | 572 | PF00244 | 0.593 |
LIG_BIR_III_4 | 44 | 48 | PF00653 | 0.587 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.489 |
LIG_CtBP_PxDLS_1 | 262 | 266 | PF00389 | 0.481 |
LIG_EH1_1 | 110 | 118 | PF00400 | 0.436 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.456 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.473 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.622 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.465 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.498 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.509 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.518 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.426 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.446 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.394 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.485 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.548 |
LIG_FHA_2 | 443 | 449 | PF00498 | 0.487 |
LIG_Integrin_isoDGR_2 | 46 | 48 | PF01839 | 0.794 |
LIG_LIR_Gen_1 | 144 | 151 | PF02991 | 0.412 |
LIG_LIR_LC3C_4 | 115 | 118 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.512 |
LIG_MLH1_MIPbox_1 | 549 | 553 | PF16413 | 0.437 |
LIG_NBox_RRM_1 | 538 | 548 | PF00076 | 0.410 |
LIG_NRBOX | 17 | 23 | PF00104 | 0.440 |
LIG_PTB_Apo_2 | 532 | 539 | PF02174 | 0.551 |
LIG_PTB_Apo_2 | 548 | 555 | PF02174 | 0.391 |
LIG_REV1ctd_RIR_1 | 551 | 561 | PF16727 | 0.491 |
LIG_SH2_PTP2 | 469 | 472 | PF00017 | 0.501 |
LIG_SH2_SRC | 469 | 472 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 143 | 147 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.515 |
LIG_SH3_1 | 327 | 333 | PF00018 | 0.508 |
LIG_SH3_1 | 361 | 367 | PF00018 | 0.558 |
LIG_SH3_1 | 412 | 418 | PF00018 | 0.564 |
LIG_SH3_2 | 197 | 202 | PF14604 | 0.534 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.577 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.584 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.508 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.556 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.579 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.491 |
LIG_SUMO_SIM_par_1 | 261 | 267 | PF11976 | 0.486 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.626 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.561 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.466 |
MOD_CDK_SPK_2 | 250 | 255 | PF00069 | 0.588 |
MOD_CDK_SPK_2 | 484 | 489 | PF00069 | 0.527 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.529 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.562 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.517 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.663 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.567 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.513 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.443 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.588 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.488 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.551 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.448 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.544 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.658 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.813 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.700 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.698 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.695 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.735 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.876 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.762 |
MOD_GlcNHglycan | 72 | 76 | PF01048 | 0.762 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.471 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.523 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.502 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.598 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.488 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.561 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.598 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.497 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.508 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.477 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.792 |
MOD_N-GLC_1 | 534 | 539 | PF02516 | 0.666 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.462 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.448 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.486 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.538 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.469 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.539 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.461 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.532 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.571 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.574 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.451 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.530 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.476 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.574 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.536 |
MOD_PKB_1 | 139 | 147 | PF00069 | 0.431 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.594 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.461 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.446 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.382 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.468 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.515 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.507 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.544 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.614 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.495 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.583 |
MOD_ProDKin_1 | 484 | 490 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 183 | 186 | PF00179 | 0.601 |
MOD_SUMO_for_1 | 494 | 497 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 407 | 414 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.494 |
TRG_DiLeu_BaEn_2 | 431 | 437 | PF01217 | 0.468 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_2 | 542 | 548 | PF01217 | 0.347 |
TRG_DiLeu_BaEn_4 | 87 | 93 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.734 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5P8 | Leptomonas seymouri | 54% | 100% |
A0A3S7X7F2 | Leishmania donovani | 26% | 99% |
A4HAF2 | Leishmania braziliensis | 78% | 100% |
A4HAF3 | Leishmania braziliensis | 26% | 99% |
A4I9K8 | Leishmania infantum | 100% | 100% |
A4I9K9 | Leishmania infantum | 27% | 99% |
E9B4K6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q3H0 | Leishmania major | 91% | 100% |