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: A4HTE6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 301 | 305 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 492 | 496 | PF00656 | 0.663 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.761 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.745 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.734 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.725 |
CLV_PCSK_PC7_1 | 500 | 506 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.664 |
DOC_CDC14_PxL_1 | 432 | 440 | PF14671 | 0.766 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.767 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.618 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.764 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.729 |
DOC_MAPK_RevD_3 | 67 | 81 | PF00069 | 0.581 |
DOC_PP2B_PxIxI_1 | 173 | 179 | PF00149 | 0.640 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.846 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.837 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.594 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.742 |
DOC_USP7_UBL2_3 | 626 | 630 | PF12436 | 0.579 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.751 |
LIG_14-3-3_CanoR_1 | 183 | 191 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 206 | 215 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 229 | 239 | PF00244 | 0.778 |
LIG_14-3-3_CanoR_1 | 370 | 375 | PF00244 | 0.819 |
LIG_14-3-3_CanoR_1 | 52 | 58 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 554 | 560 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 619 | 629 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.646 |
LIG_APCC_ABBA_1 | 559 | 564 | PF00400 | 0.612 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.720 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.678 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.690 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.809 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.739 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.744 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.664 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.757 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.715 |
LIG_Integrin_isoDGR_2 | 87 | 89 | PF01839 | 0.720 |
LIG_SH2_STAP1 | 250 | 254 | PF00017 | 0.678 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.684 |
LIG_SH3_2 | 165 | 170 | PF14604 | 0.635 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.642 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.729 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.728 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.739 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.642 |
LIG_SUMO_SIM_anti_2 | 75 | 80 | PF11976 | 0.740 |
LIG_SUMO_SIM_par_1 | 242 | 249 | PF11976 | 0.668 |
LIG_SUMO_SIM_par_1 | 436 | 441 | PF11976 | 0.723 |
LIG_TRAF2_1 | 614 | 617 | PF00917 | 0.631 |
LIG_WRC_WIRS_1 | 351 | 356 | PF05994 | 0.627 |
LIG_WW_3 | 575 | 579 | PF00397 | 0.616 |
MOD_CAAXbox | 632 | 635 | PF01239 | 0.750 |
MOD_CDC14_SPxK_1 | 575 | 578 | PF00782 | 0.701 |
MOD_CDK_SPxK_1 | 572 | 578 | PF00069 | 0.704 |
MOD_CDK_SPxxK_3 | 170 | 177 | PF00069 | 0.642 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.764 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.665 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.772 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.701 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.817 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.826 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.667 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.762 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.668 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.807 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.717 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.728 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.712 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.761 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.620 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.704 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.741 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.786 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.666 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.762 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.753 |
MOD_GlcNHglycan | 248 | 253 | PF01048 | 0.723 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.633 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.759 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.691 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.668 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.669 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.602 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.637 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.716 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.654 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.824 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.651 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.792 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.653 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.712 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.733 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.680 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.830 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.749 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.740 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.653 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.750 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.807 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.785 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.778 |
MOD_LATS_1 | 458 | 464 | PF00433 | 0.611 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.813 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.748 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.722 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.738 |
MOD_N-GLC_2 | 579 | 581 | PF02516 | 0.610 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.713 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.784 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.805 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.768 |
MOD_NEK2_2 | 252 | 257 | PF00069 | 0.672 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.583 |
MOD_NEK2_2 | 621 | 626 | PF00069 | 0.592 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.734 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.752 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.768 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.556 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.754 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.788 |
MOD_PK_1 | 65 | 71 | PF00069 | 0.616 |
MOD_PKA_1 | 221 | 227 | PF00069 | 0.726 |
MOD_PKA_1 | 509 | 515 | PF00069 | 0.631 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.652 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.664 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.726 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.716 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.729 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.725 |
MOD_Plk_1 | 298 | 304 | PF00069 | 0.610 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.766 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.627 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.641 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.609 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.704 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.629 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.727 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.652 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.640 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.822 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.780 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.590 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.764 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.717 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.752 |
MOD_SUMO_rev_2 | 419 | 426 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 512 | 518 | PF00179 | 0.660 |
TRG_DiLeu_BaEn_4 | 313 | 319 | PF01217 | 0.625 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.762 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.749 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.754 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.708 |
TRG_NLS_MonoExtC_3 | 625 | 630 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 626 | 631 | PF00514 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 257 | 261 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 605 | 609 | PF00026 | 0.723 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQ13 | Leishmania donovani | 99% | 100% |
A4H538 | Leishmania braziliensis | 26% | 100% |
E9ALA6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 98% |
Q4QIJ8 | Leishmania major | 72% | 99% |