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: E9AF50
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 159 | 163 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.282 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.485 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.468 |
DEG_APCC_DBOX_1 | 102 | 110 | PF00400 | 0.410 |
DEG_SCF_FBW7_2 | 43 | 49 | PF00400 | 0.329 |
DEG_SIAH_1 | 142 | 150 | PF03145 | 0.319 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.537 |
DOC_CKS1_1 | 43 | 48 | PF01111 | 0.426 |
DOC_CYCLIN_RxL_1 | 311 | 319 | PF00134 | 0.396 |
DOC_CYCLIN_RxL_1 | 365 | 374 | PF00134 | 0.360 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 368 | 376 | PF00134 | 0.381 |
DOC_CYCLIN_yCln2_LP_2 | 188 | 194 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 40 | 46 | PF00134 | 0.425 |
DOC_MAPK_DCC_7 | 103 | 111 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 29 | 38 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 342 | 350 | PF00069 | 0.279 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.263 |
DOC_PP1_RVXF_1 | 10 | 17 | PF00149 | 0.392 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.453 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.366 |
DOC_USP7_MATH_2 | 472 | 478 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 177 | 181 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.499 |
LIG_14-3-3_CanoR_1 | 126 | 135 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.450 |
LIG_Actin_WH2_2 | 2 | 20 | PF00022 | 0.301 |
LIG_BRCT_BRCA1_1 | 164 | 168 | PF00533 | 0.441 |
LIG_BRCT_BRCA1_1 | 283 | 287 | PF00533 | 0.297 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_2 | 164 | 170 | PF00533 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 216 | 222 | PF00928 | 0.210 |
LIG_EVH1_2 | 494 | 498 | PF00568 | 0.404 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.341 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.469 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.351 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.547 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.395 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.408 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.370 |
LIG_GBD_Chelix_1 | 175 | 183 | PF00786 | 0.365 |
LIG_LIR_Apic_2 | 443 | 449 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 220 | 230 | PF02991 | 0.253 |
LIG_LIR_Gen_1 | 231 | 242 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 365 | 370 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.309 |
LIG_NRBOX | 312 | 318 | PF00104 | 0.258 |
LIG_PCNA_PIPBox_1 | 386 | 395 | PF02747 | 0.368 |
LIG_PCNA_yPIPBox_3 | 118 | 126 | PF02747 | 0.347 |
LIG_PDZ_Class_2 | 528 | 533 | PF00595 | 0.491 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.357 |
LIG_Rb_LxCxE_1 | 123 | 139 | PF01857 | 0.449 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.407 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.399 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 459 | 462 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.279 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.325 |
LIG_SH3_3 | 137 | 143 | PF00018 | 0.463 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.273 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.333 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.344 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.566 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.385 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.381 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.478 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.300 |
LIG_SxIP_EBH_1 | 103 | 115 | PF03271 | 0.365 |
LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.404 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.291 |
MOD_CDK_SPK_2 | 133 | 138 | PF00069 | 0.410 |
MOD_CDK_SPxK_1 | 410 | 416 | PF00069 | 0.717 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.476 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.382 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.150 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.243 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.352 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.426 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.474 |
MOD_CK2_1 | 507 | 513 | PF00069 | 0.397 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.304 |
MOD_CMANNOS | 219 | 222 | PF00535 | 0.330 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.400 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.349 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.249 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.358 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.657 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.399 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.399 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.308 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.331 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.714 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.411 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.263 |
MOD_N-GLC_2 | 155 | 157 | PF02516 | 0.359 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.579 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.295 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.476 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.357 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.331 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.345 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.496 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.476 |
MOD_PK_1 | 18 | 24 | PF00069 | 0.300 |
MOD_PK_1 | 279 | 285 | PF00069 | 0.357 |
MOD_PKA_1 | 519 | 525 | PF00069 | 0.419 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.318 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.465 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.260 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.393 |
MOD_Plk_1 | 474 | 480 | PF00069 | 0.427 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.279 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.343 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.308 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.361 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.411 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.453 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.352 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.269 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.297 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.311 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.729 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.502 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.275 |
MOD_SUMO_rev_2 | 523 | 530 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_1 | 474 | 479 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P380 | Leptomonas seymouri | 56% | 100% |
A0A0S4JCU0 | Bodo saltans | 42% | 100% |
A0A1X0P6I8 | Trypanosomatidae | 47% | 100% |
A0A3Q8IG99 | Leishmania donovani | 88% | 100% |
A0A3R7KHD1 | Trypanosoma rangeli | 47% | 100% |
A4HMQ0 | Leishmania braziliensis | 72% | 100% |
A4IBB8 | Leishmania infantum | 88% | 100% |
E9B6A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5BJB2 | Trypanosoma cruzi | 46% | 100% |