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 |
Related structures:
AlphaFold database: A4HCU4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.524 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 456 | 460 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.651 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.334 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 239 | 241 | PF00082 | 0.790 |
CLV_PCSK_PC1ET2_1 | 422 | 424 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.584 |
DEG_APCC_DBOX_1 | 150 | 158 | PF00400 | 0.474 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.459 |
DEG_SPOP_SBC_1 | 135 | 139 | PF00917 | 0.649 |
DEG_SPOP_SBC_1 | 45 | 49 | PF00917 | 0.721 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.488 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.448 |
DOC_CKS1_1 | 372 | 377 | PF01111 | 0.525 |
DOC_CYCLIN_RxL_1 | 314 | 322 | PF00134 | 0.380 |
DOC_MAPK_DCC_7 | 267 | 276 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.501 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.590 |
LIG_14-3-3_CanoR_1 | 172 | 177 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 279 | 287 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 303 | 312 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 67 | 77 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 288 | 305 | PF00022 | 0.488 |
LIG_BIR_III_2 | 459 | 463 | PF00653 | 0.400 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 318 | 322 | PF01394 | 0.520 |
LIG_eIF4E_1 | 472 | 478 | PF01652 | 0.417 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.546 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.446 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.424 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.339 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.360 |
LIG_FHA_2 | 179 | 185 | PF00498 | 0.516 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.326 |
LIG_GBD_Chelix_1 | 287 | 295 | PF00786 | 0.338 |
LIG_LIR_Apic_2 | 445 | 450 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 437 | 447 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 518 | 525 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.438 |
LIG_MYND_1 | 262 | 266 | PF01753 | 0.459 |
LIG_PCNA_yPIPBox_3 | 284 | 296 | PF02747 | 0.446 |
LIG_PDZ_Class_1 | 520 | 525 | PF00595 | 0.455 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 312 | 316 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.378 |
LIG_SH3_2 | 375 | 380 | PF14604 | 0.529 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.610 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.440 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.635 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.468 |
LIG_SUMO_SIM_par_1 | 218 | 223 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 317 | 322 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 451 | 456 | PF11976 | 0.329 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.487 |
MOD_CDK_SPxxK_3 | 54 | 61 | PF00069 | 0.556 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.642 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.549 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.272 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.369 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.617 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.628 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.648 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.598 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.642 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.622 |
MOD_CMANNOS | 176 | 179 | PF00535 | 0.490 |
MOD_Cter_Amidation | 162 | 165 | PF01082 | 0.475 |
MOD_Cter_Amidation | 237 | 240 | PF01082 | 0.739 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.641 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.635 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.561 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.332 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.420 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.671 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.582 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.447 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.578 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.717 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.273 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.634 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.621 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.611 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.225 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.558 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.442 |
MOD_LATS_1 | 301 | 307 | PF00433 | 0.345 |
MOD_LATS_1 | 365 | 371 | PF00433 | 0.491 |
MOD_LATS_1 | 66 | 72 | PF00433 | 0.502 |
MOD_N-GLC_1 | 227 | 232 | PF02516 | 0.692 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.560 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.572 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.310 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.388 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.332 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.348 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.604 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.488 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.456 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.487 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.531 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.534 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.246 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.471 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.482 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.559 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.402 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.516 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.204 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.431 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.462 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.593 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.584 |
MOD_SUMO_rev_2 | 103 | 111 | PF00179 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.465 |
TRG_DiLeu_BaLyEn_6 | 314 | 319 | PF01217 | 0.195 |
TRG_DiLeu_BaLyEn_6 | 409 | 414 | PF01217 | 0.605 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.409 |
TRG_ER_diArg_1 | 144 | 147 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 164 | 166 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.682 |
TRG_NLS_MonoExtN_4 | 237 | 243 | PF00514 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 249 | 254 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 317 | 322 | PF00026 | 0.195 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I045 | Leptomonas seymouri | 62% | 89% |
A0A0S4IVC3 | Bodo saltans | 43% | 100% |
A0A1X0NWZ9 | Trypanosomatidae | 51% | 100% |
A0A3S7WXN4 | Leishmania donovani | 83% | 78% |
A0A422MX57 | Trypanosoma rangeli | 54% | 100% |
A4I0C5 | Leishmania infantum | 83% | 78% |
C9ZV46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AW89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QB89 | Leishmania major | 84% | 100% |
V5ARP5 | Trypanosoma cruzi | 52% | 100% |