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: Q4QH34
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.629 |
CLV_C14_Caspase3-7 | 579 | 583 | PF00656 | 0.631 |
CLV_MEL_PAP_1 | 69 | 75 | PF00089 | 0.796 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.637 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 608 | 610 | PF00082 | 0.724 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.729 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.657 |
DEG_APCC_DBOX_1 | 559 | 567 | PF00400 | 0.653 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.714 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.740 |
DEG_SPOP_SBC_1 | 535 | 539 | PF00917 | 0.583 |
DOC_CYCLIN_RxL_1 | 587 | 597 | PF00134 | 0.701 |
DOC_MAPK_gen_1 | 222 | 231 | PF00069 | 0.737 |
DOC_MAPK_gen_1 | 290 | 300 | PF00069 | 0.682 |
DOC_MAPK_MEF2A_6 | 293 | 302 | PF00069 | 0.605 |
DOC_PP1_RVXF_1 | 589 | 596 | PF00149 | 0.627 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.793 |
DOC_SPAK_OSR1_1 | 180 | 184 | PF12202 | 0.707 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.712 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 133 | 138 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 180 | 188 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 241 | 250 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 432 | 440 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 590 | 596 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 67 | 72 | PF00244 | 0.674 |
LIG_Actin_WH2_2 | 261 | 279 | PF00022 | 0.709 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.705 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.699 |
LIG_CaM_IQ_9 | 295 | 310 | PF13499 | 0.666 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.814 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.643 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.655 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.711 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.644 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.724 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.617 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.708 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.758 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.753 |
LIG_FHA_2 | 577 | 583 | PF00498 | 0.745 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.650 |
LIG_Integrin_isoDGR_2 | 131 | 133 | PF01839 | 0.633 |
LIG_IRF3_LxIS_1 | 294 | 301 | PF10401 | 0.651 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.696 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 630 | 636 | PF02991 | 0.704 |
LIG_MYND_1 | 169 | 173 | PF01753 | 0.686 |
LIG_NBox_RRM_1 | 615 | 625 | PF00076 | 0.647 |
LIG_PCNA_PIPBox_1 | 269 | 278 | PF02747 | 0.708 |
LIG_Pex14_1 | 213 | 217 | PF04695 | 0.621 |
LIG_PTAP_UEV_1 | 105 | 110 | PF05743 | 0.700 |
LIG_SH2_GRB2like | 547 | 550 | PF00017 | 0.698 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.707 |
LIG_SH2_PTP2 | 228 | 231 | PF00017 | 0.678 |
LIG_SH2_STAP1 | 636 | 640 | PF00017 | 0.723 |
LIG_SH2_STAT3 | 547 | 550 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.722 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 636 | 639 | PF00017 | 0.642 |
LIG_SH3_1 | 172 | 178 | PF00018 | 0.722 |
LIG_SH3_2 | 175 | 180 | PF14604 | 0.697 |
LIG_SH3_2 | 62 | 67 | PF14604 | 0.692 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.703 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.737 |
LIG_SH3_3 | 205 | 211 | PF00018 | 0.681 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.674 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.644 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.674 |
LIG_SH3_5 | 249 | 253 | PF00018 | 0.678 |
LIG_SUMO_SIM_par_1 | 456 | 462 | PF11976 | 0.615 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.673 |
LIG_TRAF2_1 | 337 | 340 | PF00917 | 0.809 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.701 |
LIG_WW_3 | 290 | 294 | PF00397 | 0.719 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.808 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.695 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.641 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.710 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.731 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.662 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.694 |
MOD_CK1_1 | 594 | 600 | PF00069 | 0.636 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.796 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.641 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.662 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.761 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.763 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.673 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.695 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.727 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.743 |
MOD_GlcNHglycan | 252 | 256 | PF01048 | 0.760 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.458 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.788 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.797 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.749 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.813 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.629 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.564 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.811 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.745 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.728 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.662 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.711 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.591 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.630 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.777 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.693 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.716 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.741 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.674 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.537 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.816 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.715 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.742 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.660 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.777 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.716 |
MOD_NEK2_2 | 636 | 641 | PF00069 | 0.727 |
MOD_PIKK_1 | 320 | 326 | PF00454 | 0.697 |
MOD_PK_1 | 133 | 139 | PF00069 | 0.722 |
MOD_PK_1 | 67 | 73 | PF00069 | 0.798 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.737 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.618 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.769 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.710 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.647 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.796 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.728 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.702 |
MOD_Plk_1 | 144 | 150 | PF00069 | 0.452 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.545 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.746 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.420 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.730 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.760 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.617 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.725 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.724 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.815 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.765 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.776 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.741 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.761 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.427 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.707 |
MOD_SUMO_for_1 | 337 | 340 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.650 |
TRG_DiLeu_BaLyEn_6 | 46 | 51 | PF01217 | 0.661 |
TRG_DiLeu_BaLyEn_6 | 588 | 593 | PF01217 | 0.622 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.678 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 276 | 278 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 296 | 298 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.709 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P315 | Leptomonas seymouri | 35% | 100% |
A0A3Q8I910 | Leishmania donovani | 92% | 100% |
A4H6G2 | Leishmania braziliensis | 73% | 97% |
A4HUV7 | Leishmania infantum | 92% | 100% |
E9ANJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |