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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AVG4
Term | Name | Level | Count |
---|---|---|---|
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003723 | RNA binding | 4 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
GO:0003729 | mRNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.528 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.349 |
DEG_SCF_FBW7_1 | 278 | 285 | PF00400 | 0.284 |
DEG_SCF_FBW7_1 | 77 | 83 | PF00400 | 0.463 |
DEG_SCF_FBW7_1 | 90 | 97 | PF00400 | 0.500 |
DOC_CDC14_PxL_1 | 414 | 422 | PF14671 | 0.347 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.563 |
DOC_CKS1_1 | 77 | 82 | PF01111 | 0.578 |
DOC_CKS1_1 | 91 | 96 | PF01111 | 0.644 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.746 |
DOC_CYCLIN_yCln2_LP_2 | 88 | 94 | PF00134 | 0.697 |
DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.762 |
DOC_PP4_FxxP_1 | 48 | 51 | PF00568 | 0.604 |
DOC_PP4_FxxP_1 | 522 | 525 | PF00568 | 0.643 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.682 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.723 |
DOC_USP7_UBL2_3 | 505 | 509 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.284 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 342 | 351 | PF00244 | 0.446 |
LIG_Actin_WH2_2 | 425 | 440 | PF00022 | 0.284 |
LIG_AP2alpha_2 | 390 | 392 | PF02296 | 0.284 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
LIG_BIR_III_4 | 318 | 322 | PF00653 | 0.300 |
LIG_BRCT_BRCA1_1 | 44 | 48 | PF00533 | 0.596 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.335 |
LIG_EH1_1 | 285 | 293 | PF00400 | 0.284 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.724 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.363 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.278 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.270 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.461 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.689 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.584 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.333 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.319 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.345 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.633 |
LIG_LIR_Apic_2 | 45 | 51 | PF02991 | 0.605 |
LIG_LIR_Apic_2 | 519 | 525 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 12 | 22 | PF02991 | 0.657 |
LIG_LIR_Gen_1 | 244 | 255 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.185 |
LIG_LIR_Gen_1 | 83 | 92 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.176 |
LIG_LIR_Nem_3 | 464 | 469 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.639 |
LIG_MAD2 | 435 | 443 | PF02301 | 0.319 |
LIG_PCNA_yPIPBox_3 | 317 | 329 | PF02747 | 0.270 |
LIG_PTB_Apo_2 | 496 | 503 | PF02174 | 0.371 |
LIG_PTB_Phospho_1 | 496 | 502 | PF10480 | 0.377 |
LIG_Rb_pABgroove_1 | 250 | 258 | PF01858 | 0.284 |
LIG_SH2_CRK | 341 | 345 | PF00017 | 0.336 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.659 |
LIG_SH2_GRB2like | 247 | 250 | PF00017 | 0.284 |
LIG_SH2_NCK_1 | 564 | 568 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 92 | 96 | PF00017 | 0.709 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 395 | 398 | PF00017 | 0.270 |
LIG_SH2_STAT3 | 469 | 472 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.723 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.321 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.552 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.333 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.366 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.699 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.597 |
LIG_SH3_4 | 36 | 43 | PF00018 | 0.656 |
LIG_SUMO_SIM_par_1 | 276 | 281 | PF11976 | 0.363 |
LIG_TRAF2_1 | 297 | 300 | PF00917 | 0.248 |
MOD_CDC14_SPxK_1 | 61 | 64 | PF00782 | 0.600 |
MOD_CDK_SPK_2 | 366 | 371 | PF00069 | 0.398 |
MOD_CDK_SPxK_1 | 58 | 64 | PF00069 | 0.687 |
MOD_CDK_SPxxK_3 | 128 | 135 | PF00069 | 0.643 |
MOD_CDK_SPxxK_3 | 366 | 373 | PF00069 | 0.373 |
MOD_CDK_SPxxK_3 | 536 | 543 | PF00069 | 0.727 |
MOD_CDK_SPxxK_3 | 94 | 101 | PF00069 | 0.729 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.643 |
MOD_CK1_1 | 185 | 191 | PF00069 | 0.561 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.664 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.692 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.662 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.276 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.680 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.700 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.629 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.504 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.593 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.652 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.657 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.537 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.304 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.333 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.421 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.698 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.628 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.539 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.664 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.619 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.394 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.693 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.645 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.710 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.289 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.635 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.524 |
MOD_PIKK_1 | 185 | 191 | PF00454 | 0.618 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.598 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.743 |
MOD_Plk_1 | 408 | 414 | PF00069 | 0.439 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.684 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.675 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.284 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.342 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.582 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.709 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.668 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.584 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.437 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 110 | 119 | PF00179 | 0.697 |
MOD_SUMO_rev_2 | 402 | 408 | PF00179 | 0.382 |
MOD_SUMO_rev_2 | 7 | 12 | PF00179 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 492 | 497 | PF01217 | 0.492 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.659 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.322 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.533 |
TRG_NLS_Bipartite_1 | 117 | 139 | PF00514 | 0.643 |
TRG_NLS_MonoExtN_4 | 132 | 139 | PF00514 | 0.650 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC50 | Leptomonas seymouri | 73% | 98% |
A0A0S4IY52 | Bodo saltans | 48% | 80% |
A0A0S4JMB8 | Bodo saltans | 32% | 81% |
A0A1X0NHM5 | Trypanosomatidae | 57% | 100% |
A0A3S7WWX7 | Leishmania donovani | 93% | 100% |
A0A422N8V0 | Trypanosoma rangeli | 54% | 100% |
A4HC32 | Leishmania braziliensis | 84% | 100% |
A4HZH4 | Leishmania infantum | 93% | 100% |
D0A0Z9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 97% |
P39016 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 66% |
Q4QC15 | Leishmania major | 92% | 100% |
V5B1W9 | Trypanosoma cruzi | 53% | 100% |