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: Q4QEQ9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 32 | 36 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.708 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.671 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.697 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.615 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.582 |
CLV_PCSK_FUR_1 | 270 | 274 | PF00082 | 0.721 |
CLV_PCSK_FUR_1 | 55 | 59 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.661 |
DEG_SCF_TRCP1_1 | 615 | 621 | PF00400 | 0.647 |
DEG_SCF_TRCP1_1 | 88 | 93 | PF00400 | 0.560 |
DOC_ANK_TNKS_1 | 573 | 580 | PF00023 | 0.649 |
DOC_MAPK_DCC_7 | 118 | 126 | PF00069 | 0.637 |
DOC_MAPK_gen_1 | 335 | 345 | PF00069 | 0.734 |
DOC_PP2B_LxvP_1 | 448 | 451 | PF13499 | 0.719 |
DOC_PP2B_LxvP_1 | 587 | 590 | PF13499 | 0.629 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.835 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.659 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 588 | 593 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 107 | 115 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 206 | 213 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 285 | 295 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 465 | 469 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 539 | 545 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 580 | 590 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 606 | 613 | PF00244 | 0.664 |
LIG_14-3-3_CterR_2 | 637 | 640 | PF00244 | 0.619 |
LIG_Actin_WH2_2 | 112 | 127 | PF00022 | 0.597 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.566 |
LIG_deltaCOP1_diTrp_1 | 188 | 200 | PF00928 | 0.585 |
LIG_deltaCOP1_diTrp_1 | 393 | 401 | PF00928 | 0.668 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.593 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.742 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.688 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.539 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.577 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.582 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.741 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.566 |
LIG_GSK3_LRP6_1 | 588 | 594 | PF00069 | 0.634 |
LIG_Integrin_isoDGR_2 | 368 | 370 | PF01839 | 0.603 |
LIG_Integrin_isoDGR_2 | 622 | 624 | PF01839 | 0.655 |
LIG_LIR_Apic_2 | 135 | 141 | PF02991 | 0.680 |
LIG_LIR_Apic_2 | 177 | 183 | PF02991 | 0.613 |
LIG_LIR_Apic_2 | 444 | 450 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.681 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.596 |
LIG_SH2_GRB2like | 418 | 421 | PF00017 | 0.669 |
LIG_SH2_STAT3 | 264 | 267 | PF00017 | 0.692 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.614 |
LIG_SH3_1 | 163 | 169 | PF00018 | 0.668 |
LIG_SH3_1 | 233 | 239 | PF00018 | 0.821 |
LIG_SH3_1 | 447 | 453 | PF00018 | 0.659 |
LIG_SH3_1 | 96 | 102 | PF00018 | 0.697 |
LIG_SH3_2 | 11 | 16 | PF14604 | 0.569 |
LIG_SH3_2 | 632 | 637 | PF14604 | 0.690 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.717 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.815 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.654 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.593 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.731 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.777 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.775 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.693 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.635 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.620 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.694 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.697 |
LIG_SUMO_SIM_anti_2 | 42 | 48 | PF11976 | 0.594 |
LIG_SUMO_SIM_par_1 | 109 | 117 | PF11976 | 0.590 |
LIG_TRFH_1 | 180 | 184 | PF08558 | 0.668 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.799 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.657 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.641 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.694 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.806 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.656 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.761 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.673 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.736 |
MOD_CK1_1 | 591 | 597 | PF00069 | 0.707 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.641 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.692 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.533 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.662 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.580 |
MOD_CK2_1 | 605 | 611 | PF00069 | 0.740 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.688 |
MOD_Cter_Amidation | 521 | 524 | PF01082 | 0.587 |
MOD_Cter_Amidation | 622 | 625 | PF01082 | 0.654 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.757 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.826 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.774 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.783 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.736 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.648 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.506 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.609 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.630 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.641 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.596 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.635 |
MOD_GlcNHglycan | 614 | 618 | PF01048 | 0.699 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.752 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.661 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.609 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.760 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.722 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.740 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.650 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.670 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.702 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.700 |
MOD_LATS_1 | 156 | 162 | PF00433 | 0.654 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.736 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.521 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.708 |
MOD_N-GLC_1 | 547 | 552 | PF02516 | 0.583 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.710 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.654 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.660 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.650 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.707 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.641 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.693 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.736 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.675 |
MOD_PIKK_1 | 605 | 611 | PF00454 | 0.599 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.666 |
MOD_PKA_1 | 285 | 291 | PF00069 | 0.674 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.637 |
MOD_PKA_1 | 523 | 529 | PF00069 | 0.693 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.691 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.732 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.654 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.601 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.580 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.822 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.579 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.695 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.745 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.666 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.594 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.692 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.600 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.603 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.521 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.646 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.649 |
MOD_Plk_2-3 | 220 | 226 | PF00069 | 0.533 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.594 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.634 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.589 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.704 |
MOD_Plk_4 | 549 | 555 | PF00069 | 0.595 |
MOD_Plk_4 | 596 | 602 | PF00069 | 0.549 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.756 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.663 |
MOD_ProDKin_1 | 588 | 594 | PF00069 | 0.682 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.570 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.698 |
TRG_ER_diArg_1 | 56 | 59 | PF00400 | 0.687 |
TRG_NES_CRM1_1 | 561 | 572 | PF08389 | 0.553 |
TRG_NLS_MonoExtC_3 | 522 | 527 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 521 | 528 | PF00514 | 0.690 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDQ3 | Leishmania donovani | 85% | 100% |
A4H8N4 | Leishmania braziliensis | 51% | 100% |
A4HX04 | Leishmania infantum | 84% | 100% |
E9AQR7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |