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: A4H5N6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.593 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.523 |
CLV_PCSK_FUR_1 | 146 | 150 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 518 | 520 | PF00082 | 0.572 |
CLV_PCSK_PC7_1 | 112 | 118 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.566 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.570 |
DEG_SPOP_SBC_1 | 71 | 75 | PF00917 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 20 | 26 | PF00134 | 0.660 |
DOC_MAPK_DCC_7 | 400 | 408 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 28 | 37 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 400 | 408 | PF00069 | 0.535 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.685 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.671 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.663 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.683 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 256 | 260 | PF00244 | 0.585 |
LIG_Actin_WH2_2 | 85 | 101 | PF00022 | 0.612 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.440 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.569 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.685 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.775 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 369 | 374 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 491 | 500 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 491 | 495 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.466 |
LIG_PDZ_Class_1 | 519 | 524 | PF00595 | 0.489 |
LIG_PDZ_Wminus1_1 | 522 | 524 | PF00595 | 0.653 |
LIG_PTB_Apo_2 | 56 | 63 | PF02174 | 0.688 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.605 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.586 |
LIG_SH2_GRB2like | 358 | 361 | PF00017 | 0.468 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.613 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.505 |
LIG_SH2_SRC | 358 | 361 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.550 |
LIG_SH3_2 | 442 | 447 | PF14604 | 0.666 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.608 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.656 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.609 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.690 |
LIG_SH3_CIN85_PxpxPR_1 | 442 | 447 | PF14604 | 0.666 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.598 |
LIG_TRAF2_1 | 141 | 144 | PF00917 | 0.559 |
LIG_TYR_ITIM | 490 | 495 | PF00017 | 0.570 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.568 |
LIG_WW_3 | 444 | 448 | PF00397 | 0.672 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.602 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.644 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.668 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.562 |
MOD_CK1_1 | 491 | 497 | PF00069 | 0.604 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.666 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.709 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.675 |
MOD_Cter_Amidation | 516 | 519 | PF01082 | 0.570 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.614 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.611 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.692 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.661 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.489 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.548 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.504 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.727 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.640 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.761 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.660 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.805 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.638 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.569 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.570 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.658 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.482 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.549 |
MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.639 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.601 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.554 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.570 |
MOD_NEK2_2 | 200 | 205 | PF00069 | 0.434 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.731 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.478 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.492 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.708 |
MOD_PKA_1 | 283 | 289 | PF00069 | 0.531 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.448 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.470 |
MOD_PKA_2 | 255 | 261 | PF00069 | 0.584 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.605 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.683 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.627 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.492 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.462 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.526 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.685 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.387 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.469 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.566 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.661 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.520 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.788 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.475 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.768 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.648 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.617 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.502 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.614 |
MOD_SUMO_for_1 | 126 | 129 | PF00179 | 0.483 |
MOD_SUMO_for_1 | 141 | 144 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 45 | 54 | PF00179 | 0.608 |
MOD_SUMO_rev_2 | 478 | 485 | PF00179 | 0.609 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 492 | 495 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.545 |
TRG_NLS_MonoExtN_4 | 115 | 120 | PF00514 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J5 | Leptomonas seymouri | 45% | 100% |
A0A3Q8IBX4 | Leishmania donovani | 74% | 100% |
A4HU08 | Leishmania infantum | 74% | 100% |
E9AMT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QHT7 | Leishmania major | 72% | 100% |