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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H760
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0008168 | methyltransferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.672 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.564 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 109 | 111 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 143 | 145 | PF00082 | 0.741 |
CLV_PCSK_PC7_1 | 105 | 111 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.409 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.691 |
DEG_SPOP_SBC_1 | 137 | 141 | PF00917 | 0.714 |
DOC_CYCLIN_yCln2_LP_2 | 272 | 278 | PF00134 | 0.416 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.406 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.371 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.768 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 202 | 211 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 435 | 440 | PF00244 | 0.580 |
LIG_BIR_III_2 | 287 | 291 | PF00653 | 0.487 |
LIG_BIR_III_4 | 433 | 437 | PF00653 | 0.538 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.397 |
LIG_Clathr_ClatBox_1 | 294 | 298 | PF01394 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 419 | 426 | PF00928 | 0.492 |
LIG_DLG_GKlike_1 | 3 | 11 | PF00625 | 0.547 |
LIG_eIF4E_1 | 225 | 231 | PF01652 | 0.341 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.467 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.513 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.485 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.573 |
LIG_FHA_2 | 380 | 386 | PF00498 | 0.408 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.454 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.590 |
LIG_LIR_Apic_2 | 227 | 232 | PF02991 | 0.343 |
LIG_LIR_Apic_2 | 446 | 450 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 458 | 466 | PF02991 | 0.520 |
LIG_LIR_LC3C_4 | 366 | 371 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.483 |
LIG_PCNA_PIPBox_1 | 372 | 381 | PF02747 | 0.469 |
LIG_Pex14_1 | 262 | 266 | PF04695 | 0.440 |
LIG_Pex14_1 | 443 | 447 | PF04695 | 0.498 |
LIG_REV1ctd_RIR_1 | 312 | 322 | PF16727 | 0.508 |
LIG_SH2_PTP2 | 447 | 450 | PF00017 | 0.447 |
LIG_SH2_SRC | 181 | 184 | PF00017 | 0.392 |
LIG_SH2_SRC | 447 | 450 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 38 | 41 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.479 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.464 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.498 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.400 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.742 |
LIG_SUMO_SIM_anti_2 | 365 | 373 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 245 | 252 | PF11976 | 0.431 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.648 |
LIG_UBA3_1 | 7 | 12 | PF00899 | 0.531 |
LIG_WRC_WIRS_1 | 414 | 419 | PF05994 | 0.496 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.690 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.475 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.613 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.775 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.588 |
MOD_CK2_1 | 379 | 385 | PF00069 | 0.381 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.416 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.712 |
MOD_DYRK1A_RPxSP_1 | 144 | 148 | PF00069 | 0.710 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.622 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.643 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.688 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.485 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.462 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.696 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.816 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.584 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.675 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.717 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.341 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.520 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.710 |
MOD_LATS_1 | 484 | 490 | PF00433 | 0.594 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.665 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.500 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.503 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.481 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.507 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.370 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.346 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.450 |
MOD_PK_1 | 246 | 252 | PF00069 | 0.481 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.591 |
MOD_PKB_1 | 144 | 152 | PF00069 | 0.721 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.528 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.478 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.384 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.398 |
MOD_Plk_2-3 | 472 | 478 | PF00069 | 0.702 |
MOD_Plk_2-3 | 82 | 88 | PF00069 | 0.569 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.478 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.655 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.450 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.405 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.731 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.743 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.425 |
MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.611 |
MOD_SUMO_rev_2 | 185 | 195 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 335 | 342 | PF00179 | 0.493 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.431 |
TRG_NLS_MonoExtC_3 | 108 | 113 | PF00514 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 464 | 469 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I161 | Leptomonas seymouri | 47% | 100% |
A0A0S4IWK0 | Bodo saltans | 26% | 100% |
A0A1X0P685 | Trypanosomatidae | 32% | 99% |
A0A3R7KFJ2 | Trypanosoma rangeli | 31% | 100% |
A4HA32 | Leishmania braziliensis | 74% | 99% |
A4HY95 | Leishmania infantum | 99% | 100% |
D0A0M9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AS27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QDE6 | Leishmania major | 92% | 100% |
V5B315 | Trypanosoma cruzi | 30% | 100% |