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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWU7
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016874 | ligase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.496 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 26 | 28 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.680 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.603 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.530 |
DEG_COP1_1 | 205 | 215 | PF00400 | 0.649 |
DEG_SCF_FBW7_1 | 4 | 10 | PF00400 | 0.453 |
DOC_CDC14_PxL_1 | 479 | 487 | PF14671 | 0.550 |
DOC_CKS1_1 | 144 | 149 | PF01111 | 0.541 |
DOC_CKS1_1 | 4 | 9 | PF01111 | 0.456 |
DOC_MAPK_DCC_7 | 477 | 487 | PF00069 | 0.530 |
DOC_MAPK_gen_1 | 319 | 325 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 432 | 441 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 307 | 314 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 432 | 441 | PF00069 | 0.502 |
DOC_MAPK_NFAT4_5 | 307 | 315 | PF00069 | 0.447 |
DOC_PP2B_LxvP_1 | 315 | 318 | PF13499 | 0.466 |
DOC_PP4_FxxP_1 | 141 | 144 | PF00568 | 0.643 |
DOC_PP4_FxxP_1 | 387 | 390 | PF00568 | 0.467 |
DOC_PP4_FxxP_1 | 480 | 483 | PF00568 | 0.530 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.675 |
DOC_USP7_UBL2_3 | 444 | 448 | PF12436 | 0.530 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.575 |
LIG_Actin_WH2_2 | 357 | 373 | PF00022 | 0.372 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.607 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.581 |
LIG_BIR_III_2 | 457 | 461 | PF00653 | 0.515 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 452 | 456 | PF00533 | 0.467 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.579 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.284 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.466 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.453 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.501 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.703 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.597 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.372 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.574 |
LIG_LIR_Apic_2 | 384 | 390 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 17 | 24 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 178 | 185 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 230 | 241 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 137 | 141 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.669 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.465 |
LIG_PDZ_Class_2 | 503 | 508 | PF00595 | 0.465 |
LIG_Pex14_2 | 334 | 338 | PF04695 | 0.530 |
LIG_PTB_Apo_2 | 132 | 139 | PF02174 | 0.503 |
LIG_PTB_Phospho_1 | 132 | 138 | PF10480 | 0.499 |
LIG_SH2_STAP1 | 87 | 91 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.523 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.632 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.530 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.585 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.665 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.465 |
LIG_SH3_CIN85_PxpxPR_1 | 147 | 152 | PF14604 | 0.599 |
LIG_SUMO_SIM_anti_2 | 311 | 316 | PF11976 | 0.550 |
LIG_SUMO_SIM_anti_2 | 360 | 365 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.435 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.566 |
LIG_TRAF2_1 | 464 | 467 | PF00917 | 0.467 |
LIG_TRFH_1 | 79 | 83 | PF08558 | 0.535 |
LIG_TYR_ITIM | 395 | 400 | PF00017 | 0.447 |
LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.530 |
LIG_WW_3 | 55 | 59 | PF00397 | 0.437 |
MOD_CDK_SPxxK_3 | 143 | 150 | PF00069 | 0.541 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.553 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.561 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.588 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.372 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.498 |
MOD_Cter_Amidation | 47 | 50 | PF01082 | 0.696 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.772 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.679 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.321 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.302 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.315 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.278 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.604 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.525 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.532 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.533 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.611 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.517 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.433 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.655 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.265 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.172 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.492 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.582 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.536 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.389 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.504 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.447 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.502 |
MOD_NEK2_2 | 502 | 507 | PF00069 | 0.467 |
MOD_OFUCOSY | 114 | 121 | PF10250 | 0.483 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.620 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.418 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.627 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.573 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.465 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.457 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.520 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.553 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.504 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.530 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.447 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.502 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.721 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.638 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.591 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.547 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.541 |
MOD_SUMO_rev_2 | 474 | 479 | PF00179 | 0.372 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.575 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 49 | 51 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.508 |
TRG_NES_CRM1_1 | 72 | 84 | PF08389 | 0.433 |
TRG_NLS_Bipartite_1 | 434 | 451 | PF00514 | 0.515 |
TRG_NLS_MonoExtN_4 | 444 | 451 | PF00514 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 459 | 463 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 477 | 481 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5X3 | Leptomonas seymouri | 58% | 100% |
A0A3S7WYE0 | Leishmania donovani | 90% | 86% |
A0A422MP50 | Trypanosoma rangeli | 26% | 100% |
A4HDG2 | Leishmania braziliensis | 76% | 100% |
A4I0U3 | Leishmania infantum | 90% | 86% |
C9ZVE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4QAM7 | Leishmania major | 88% | 100% |
V5B5P9 | Trypanosoma cruzi | 25% | 100% |