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: A4I8M0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.520 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.581 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.594 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.509 |
DEG_APCC_DBOX_1 | 216 | 224 | PF00400 | 0.522 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.716 |
DEG_SPOP_SBC_1 | 359 | 363 | PF00917 | 0.708 |
DOC_CYCLIN_RxL_1 | 112 | 121 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 213 | 224 | PF00134 | 0.543 |
DOC_PP1_RVXF_1 | 114 | 121 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 452 | 455 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.445 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 338 | 345 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.581 |
LIG_Actin_WH2_2 | 457 | 475 | PF00022 | 0.532 |
LIG_BIR_III_4 | 121 | 125 | PF00653 | 0.493 |
LIG_BIR_III_4 | 289 | 293 | PF00653 | 0.534 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.494 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.676 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.451 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.656 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.671 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.652 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.626 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.574 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.590 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.381 |
LIG_HCF-1_HBM_1 | 200 | 203 | PF13415 | 0.532 |
LIG_LIR_Apic_2 | 450 | 455 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 117 | 125 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 393 | 400 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 393 | 399 | PF02991 | 0.544 |
LIG_Pex14_2 | 51 | 55 | PF04695 | 0.413 |
LIG_SH2_NCK_1 | 262 | 266 | PF00017 | 0.601 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.672 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.500 |
LIG_SH3_2 | 33 | 38 | PF14604 | 0.416 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.571 |
LIG_SH3_3 | 417 | 423 | PF00018 | 0.631 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.593 |
LIG_SUMO_SIM_anti_2 | 291 | 297 | PF11976 | 0.621 |
LIG_TRAF2_1 | 126 | 129 | PF00917 | 0.714 |
LIG_TRAF2_1 | 371 | 374 | PF00917 | 0.638 |
MOD_CDK_SPxxK_3 | 147 | 154 | PF00069 | 0.635 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.700 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.709 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.696 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.620 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.627 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.633 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.677 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.573 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.546 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.698 |
MOD_GlcNHglycan | 257 | 261 | PF01048 | 0.722 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.694 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.606 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.534 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.449 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.511 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.680 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.513 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.568 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.658 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.510 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.741 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.556 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.502 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.453 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.384 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.602 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.492 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.355 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.478 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.484 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.614 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.624 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.624 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.638 |
MOD_PIKK_1 | 54 | 60 | PF00454 | 0.606 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.665 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.632 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.711 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.465 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.613 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.360 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.624 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.480 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.710 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.645 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.621 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.645 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.554 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.650 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.508 |
MOD_SUMO_rev_2 | 466 | 475 | PF00179 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.639 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.507 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.693 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.749 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKK4 | Leptomonas seymouri | 58% | 99% |
A0A0S4JPU3 | Bodo saltans | 34% | 95% |
A0A3S7X6B5 | Leishmania donovani | 100% | 100% |
A0A422NYF9 | Trypanosoma rangeli | 44% | 100% |
A4HL40 | Leishmania braziliensis | 79% | 100% |
C9ZPU4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 98% |
E9B3I1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q4L9 | Leishmania major | 92% | 100% |
V5AUZ3 | Trypanosoma cruzi | 47% | 100% |