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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7WQN2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 648 | 652 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.715 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 473 | 475 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.733 |
CLV_PCSK_FUR_1 | 403 | 407 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.737 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 641 | 643 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.636 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.575 |
DEG_SCF_FBW7_1 | 19 | 24 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 421 | 425 | PF00917 | 0.721 |
DOC_ANK_TNKS_1 | 357 | 364 | PF00023 | 0.413 |
DOC_CKS1_1 | 318 | 323 | PF01111 | 0.717 |
DOC_CKS1_1 | 493 | 498 | PF01111 | 0.548 |
DOC_CKS1_1 | 511 | 516 | PF01111 | 0.628 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.588 |
DOC_PP1_RVXF_1 | 639 | 646 | PF00149 | 0.686 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.670 |
DOC_PP4_FxxP_1 | 613 | 616 | PF00568 | 0.696 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 126 | 130 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 221 | 228 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 277 | 286 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 329 | 336 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 406 | 415 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 441 | 447 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 605 | 609 | PF00244 | 0.671 |
LIG_Actin_WH2_2 | 124 | 142 | PF00022 | 0.554 |
LIG_Actin_WH2_2 | 591 | 607 | PF00022 | 0.565 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 568 | 572 | PF00533 | 0.739 |
LIG_Clathr_ClatBox_1 | 54 | 58 | PF01394 | 0.653 |
LIG_deltaCOP1_diTrp_1 | 584 | 587 | PF00928 | 0.619 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.557 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.458 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.419 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.563 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.677 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.488 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.488 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.641 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.753 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.753 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.403 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.688 |
LIG_LIR_Apic_2 | 612 | 616 | PF02991 | 0.698 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 100 | 111 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 263 | 274 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 370 | 380 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.403 |
LIG_MYND_3 | 271 | 275 | PF01753 | 0.596 |
LIG_NRP_CendR_1 | 653 | 656 | PF00754 | 0.674 |
LIG_PTB_Apo_2 | 483 | 490 | PF02174 | 0.583 |
LIG_PTB_Phospho_1 | 483 | 489 | PF10480 | 0.583 |
LIG_SH2_CRK | 196 | 200 | PF00017 | 0.554 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.633 |
LIG_SH2_NCK_1 | 99 | 103 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.739 |
LIG_SH2_STAT3 | 336 | 339 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 518 | 521 | PF00017 | 0.687 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.580 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.613 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.595 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.451 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 504 | 509 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 453 | 459 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 53 | 58 | PF11976 | 0.657 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.373 |
LIG_WRC_WIRS_1 | 95 | 100 | PF05994 | 0.596 |
MOD_CDK_SPK_2 | 527 | 532 | PF00069 | 0.561 |
MOD_CDK_SPxK_1 | 492 | 498 | PF00069 | 0.549 |
MOD_CDK_SPxK_1 | 510 | 516 | PF00069 | 0.628 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.633 |
MOD_CDK_SPxxK_3 | 527 | 534 | PF00069 | 0.499 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.578 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.725 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.729 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.690 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.502 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.694 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.805 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.415 |
MOD_Cter_Amidation | 403 | 406 | PF01082 | 0.732 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.601 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.720 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.643 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.630 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.713 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.582 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.555 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.507 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.579 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.609 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.662 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.540 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.519 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.579 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.661 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.565 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.544 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.560 |
MOD_GSK3_1 | 567 | 574 | PF00069 | 0.618 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.612 |
MOD_LATS_1 | 219 | 225 | PF00433 | 0.699 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.792 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.603 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.622 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.729 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.628 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.528 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.634 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.657 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.500 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.673 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.451 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.601 |
MOD_PIKK_1 | 148 | 154 | PF00454 | 0.584 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.738 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.580 |
MOD_PIKK_1 | 383 | 389 | PF00454 | 0.600 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.649 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.598 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.728 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.646 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.674 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.678 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.303 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.439 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.480 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.693 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.676 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.756 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.668 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.647 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.663 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.750 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.549 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.628 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.494 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.634 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.745 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.591 |
TRG_DiLeu_BaEn_1 | 141 | 146 | PF01217 | 0.265 |
TRG_DiLeu_BaLyEn_6 | 541 | 546 | PF01217 | 0.689 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.586 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.731 |
TRG_ER_diArg_1 | 640 | 643 | PF00400 | 0.666 |
TRG_NES_CRM1_1 | 125 | 137 | PF08389 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC90 | Leptomonas seymouri | 60% | 88% |
A0A1X0NNC0 | Trypanosomatidae | 32% | 100% |
A0A3R7NXN4 | Trypanosoma rangeli | 34% | 100% |
A4H5P3 | Leishmania braziliensis | 81% | 100% |
A4HTY3 | Leishmania infantum | 99% | 100% |
D0A9D9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AMR3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4QHW2 | Leishmania major | 94% | 99% |
V5DJH4 | Trypanosoma cruzi | 35% | 100% |