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: A4I2N9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.607 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.383 |
CLV_PCSK_FUR_1 | 358 | 362 | PF00082 | 0.522 |
CLV_PCSK_FUR_1 | 564 | 568 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.676 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.636 |
CLV_PCSK_PC7_1 | 319 | 325 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 562 | 568 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.675 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.649 |
DEG_SCF_FBW7_1 | 187 | 194 | PF00400 | 0.589 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.679 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.570 |
DOC_CYCLIN_RxL_1 | 360 | 373 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 230 | 236 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 155 | 164 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 319 | 329 | PF00069 | 0.599 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 349 | 356 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 483 | 492 | PF00069 | 0.634 |
DOC_PP2B_LxvP_1 | 138 | 141 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 230 | 233 | PF13499 | 0.579 |
DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.641 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.739 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 172 | 178 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 301 | 311 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 385 | 391 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 402 | 408 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 527 | 534 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 556 | 565 | PF00244 | 0.616 |
LIG_BRCT_BRCA1_1 | 545 | 549 | PF00533 | 0.564 |
LIG_FAT_LD_1 | 50 | 58 | PF03623 | 0.455 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.531 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.489 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.613 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.661 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.493 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.488 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.550 |
LIG_LIR_Apic_2 | 403 | 408 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 196 | 207 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.553 |
LIG_Pex14_1 | 353 | 357 | PF04695 | 0.422 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.447 |
LIG_SH2_CRK | 405 | 409 | PF00017 | 0.585 |
LIG_SH2_GRB2like | 203 | 206 | PF00017 | 0.560 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 234 | 238 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 405 | 409 | PF00017 | 0.585 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.545 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 419 | 422 | PF00017 | 0.739 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.537 |
LIG_SH3_1 | 405 | 411 | PF00018 | 0.604 |
LIG_SH3_2 | 522 | 527 | PF14604 | 0.632 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.536 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.690 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.550 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.634 |
LIG_SUMO_SIM_anti_2 | 35 | 40 | PF11976 | 0.630 |
LIG_SUMO_SIM_anti_2 | 487 | 492 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 484 | 489 | PF11976 | 0.633 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.612 |
LIG_WW_3 | 152 | 156 | PF00397 | 0.478 |
MOD_CDC14_SPxK_1 | 524 | 527 | PF00782 | 0.640 |
MOD_CDK_SPxK_1 | 521 | 527 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 521 | 528 | PF00069 | 0.636 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.665 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.582 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.629 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.488 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.704 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.562 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.511 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.610 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.599 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.593 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.564 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.456 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.500 |
MOD_Cter_Amidation | 43 | 46 | PF01082 | 0.584 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.644 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.563 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.478 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.576 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.720 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.577 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.412 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.568 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.699 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.671 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.680 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.568 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.497 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.475 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.592 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.712 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.630 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.559 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.727 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.746 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.610 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.536 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.608 |
MOD_N-GLC_1 | 512 | 517 | PF02516 | 0.668 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.567 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.419 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.322 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.716 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.599 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.632 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.668 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.545 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.530 |
MOD_NEK2_2 | 270 | 275 | PF00069 | 0.498 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.489 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.557 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.580 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.571 |
MOD_PIKK_1 | 492 | 498 | PF00454 | 0.630 |
MOD_PK_1 | 527 | 533 | PF00069 | 0.647 |
MOD_PKA_1 | 322 | 328 | PF00069 | 0.481 |
MOD_PKA_1 | 527 | 533 | PF00069 | 0.647 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.423 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.477 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.648 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.601 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.556 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.690 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.775 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.519 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.468 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.640 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.487 |
MOD_Plk_2-3 | 475 | 481 | PF00069 | 0.612 |
MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.585 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.529 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.477 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.471 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.482 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.495 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.744 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.678 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.523 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.521 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.633 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.603 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.544 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.565 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.481 |
TRG_ER_diArg_1 | 562 | 565 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.500 |
TRG_NES_CRM1_1 | 479 | 493 | PF08389 | 0.628 |
TRG_NLS_MonoExtC_3 | 561 | 566 | PF00514 | 0.677 |
TRG_NLS_MonoExtN_4 | 562 | 567 | PF00514 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Z3 | Leptomonas seymouri | 53% | 100% |
A0A3S7X0J7 | Leishmania donovani | 100% | 100% |
A4HFK7 | Leishmania braziliensis | 74% | 100% |
E9AD62 | Leishmania major | 92% | 100% |
E9AYY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |