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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q1K2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.701 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.571 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 555 | 557 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 420 | 424 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.801 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 196 | 198 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 534 | 536 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 497 | 501 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.659 |
DEG_APCC_DBOX_1 | 555 | 563 | PF00400 | 0.561 |
DEG_Kelch_Keap1_1 | 94 | 99 | PF01344 | 0.670 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.592 |
DOC_CYCLIN_yClb3_PxF_3 | 578 | 584 | PF00134 | 0.619 |
DOC_MAPK_FxFP_2 | 575 | 578 | PF00069 | 0.626 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 570 | 573 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.644 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 493 | 497 | PF12436 | 0.626 |
DOC_USP7_UBL2_3 | 510 | 514 | PF12436 | 0.615 |
DOC_USP7_UBL2_3 | 549 | 553 | PF12436 | 0.696 |
DOC_USP7_UBL2_3 | 557 | 561 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 204 | 213 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 492 | 496 | PF00244 | 0.534 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.652 |
LIG_BIR_III_2 | 275 | 279 | PF00653 | 0.533 |
LIG_BIR_III_4 | 433 | 437 | PF00653 | 0.657 |
LIG_EVH1_1 | 570 | 574 | PF00568 | 0.653 |
LIG_EVH1_1 | 577 | 581 | PF00568 | 0.594 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.613 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.514 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.587 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.572 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.700 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.589 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.622 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 457 | 467 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 494 | 503 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 494 | 498 | PF02991 | 0.537 |
LIG_NRBOX | 219 | 225 | PF00104 | 0.702 |
LIG_Pex14_1 | 491 | 495 | PF04695 | 0.537 |
LIG_Pex14_2 | 250 | 254 | PF04695 | 0.626 |
LIG_RPA_C_Fungi | 466 | 478 | PF08784 | 0.564 |
LIG_SH2_CRK | 495 | 499 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.538 |
LIG_SH3_2 | 10 | 15 | PF14604 | 0.657 |
LIG_SH3_2 | 228 | 233 | PF14604 | 0.634 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.659 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.530 |
LIG_SH3_3 | 568 | 574 | PF00018 | 0.645 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.598 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.795 |
LIG_TRAF2_1 | 527 | 530 | PF00917 | 0.645 |
LIG_TRAF2_1 | 72 | 75 | PF00917 | 0.631 |
LIG_TRAF2_1 | 97 | 100 | PF00917 | 0.670 |
LIG_TRFH_1 | 570 | 574 | PF08558 | 0.569 |
MOD_CDK_SPK_2 | 292 | 297 | PF00069 | 0.585 |
MOD_CDK_SPK_2 | 377 | 382 | PF00069 | 0.517 |
MOD_CDK_SPxK_1 | 227 | 233 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 292 | 299 | PF00069 | 0.627 |
MOD_CDK_SPxxK_3 | 355 | 362 | PF00069 | 0.578 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.664 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.530 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.568 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.642 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.697 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.614 |
MOD_Cter_Amidation | 508 | 511 | PF01082 | 0.635 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.539 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.789 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.625 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.761 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.685 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.611 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.659 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.656 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.722 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.766 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.644 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.462 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.489 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.575 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.574 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.545 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.504 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.574 |
MOD_PIKK_1 | 204 | 210 | PF00454 | 0.605 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.542 |
MOD_PIKK_1 | 375 | 381 | PF00454 | 0.527 |
MOD_PK_1 | 277 | 283 | PF00069 | 0.651 |
MOD_PKA_1 | 204 | 210 | PF00069 | 0.605 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.538 |
MOD_PKA_1 | 396 | 402 | PF00069 | 0.609 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.753 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.713 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.691 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.458 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.545 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.706 |
MOD_PKB_1 | 421 | 429 | PF00069 | 0.546 |
MOD_Plk_1 | 484 | 490 | PF00069 | 0.502 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.573 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.609 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.660 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.493 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.627 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.657 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.572 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 552 | 555 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 270 | 279 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 389 | 399 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 442 | 451 | PF00179 | 0.637 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.605 |
TRG_DiLeu_BaEn_3 | 149 | 155 | PF01217 | 0.634 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.744 |
TRG_ENDOCYTIC_2 | 495 | 498 | PF00928 | 0.539 |
TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 296 | 299 | PF00400 | 0.780 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.599 |
TRG_NLS_MonoExtN_4 | 420 | 425 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 233 | 237 | PF00026 | 0.679 |
TRG_Pf-PMV_PEXEL_1 | 325 | 329 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XAV9 | Leishmania donovani | 89% | 100% |
A4HP88 | Leishmania braziliensis | 64% | 99% |
A4IDJ3 | Leishmania infantum | 89% | 100% |
E9ASZ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |