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: Q4QIM9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.482 |
CLV_PCSK_PC7_1 | 371 | 377 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.447 |
CLV_Separin_Metazoa | 601 | 605 | PF03568 | 0.472 |
DEG_APCC_DBOX_1 | 15 | 23 | PF00400 | 0.498 |
DEG_APCC_DBOX_1 | 220 | 228 | PF00400 | 0.529 |
DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.529 |
DEG_SPOP_SBC_1 | 251 | 255 | PF00917 | 0.568 |
DEG_SPOP_SBC_1 | 499 | 503 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.632 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.675 |
DOC_PP2B_LxvP_1 | 264 | 267 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 57 | 60 | PF13499 | 0.514 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 500 | 504 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.467 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 36 | 44 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 376 | 385 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 374 | 391 | PF00022 | 0.456 |
LIG_Actin_WH2_2 | 535 | 551 | PF00022 | 0.505 |
LIG_BRCT_BRCA1_1 | 161 | 165 | PF00533 | 0.561 |
LIG_EVH1_1 | 266 | 270 | PF00568 | 0.623 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.524 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.707 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.688 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.544 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.440 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.499 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.457 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.660 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.475 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.387 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.388 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.514 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.619 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.556 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 115 | 123 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.608 |
LIG_PCNA_yPIPBox_3 | 580 | 592 | PF02747 | 0.433 |
LIG_Pex14_2 | 165 | 169 | PF04695 | 0.566 |
LIG_PTAP_UEV_1 | 612 | 617 | PF05743 | 0.566 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.631 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.562 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.594 |
LIG_SH3_3 | 554 | 560 | PF00018 | 0.627 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.553 |
LIG_SUMO_SIM_par_1 | 559 | 565 | PF11976 | 0.625 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.511 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.544 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.639 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.540 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.434 |
LIG_UBA3_1 | 19 | 25 | PF00899 | 0.502 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.691 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.530 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.708 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.668 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.686 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.374 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.618 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.530 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.663 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.420 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.521 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.658 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.473 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.541 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.619 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.373 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.522 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.535 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.423 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.653 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.602 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.402 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.713 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.627 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.499 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.695 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.656 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.497 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.469 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.399 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.528 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.567 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.535 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.585 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.548 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.655 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.504 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.510 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.637 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.579 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.730 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.580 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.629 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.652 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.510 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.450 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.483 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.513 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.550 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.578 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.619 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.447 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.558 |
MOD_PK_1 | 448 | 454 | PF00069 | 0.452 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.539 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.611 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.675 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.521 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.581 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.426 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.469 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.687 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.622 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.652 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.646 |
MOD_SUMO_rev_2 | 443 | 447 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 501 | 509 | PF00179 | 0.610 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 586 | 588 | PF00400 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 142 | 147 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 376 | 380 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 461 | 466 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WPV9 | Leishmania donovani | 87% | 97% |
A0A422N655 | Trypanosoma rangeli | 28% | 100% |
A4H513 | Leishmania braziliensis | 60% | 100% |
A4HT87 | Leishmania infantum | 87% | 97% |
E9AL75 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |