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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: E9B732
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010033 | response to organic substance | 3 | 1 |
GO:0010243 | response to organonitrogen compound | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0036503 | ERAD pathway | 5 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901698 | response to nitrogen compound | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 286 | 290 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.323 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 70 | 72 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.240 |
DEG_APCC_DBOX_1 | 41 | 49 | PF00400 | 0.523 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.555 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DEG_SCF_FBW7_1 | 17 | 24 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.575 |
DEG_SPOP_SBC_1 | 284 | 288 | PF00917 | 0.739 |
DOC_MAPK_gen_1 | 474 | 483 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 207 | 213 | PF00149 | 0.361 |
DOC_PP2B_LxvP_1 | 330 | 333 | PF13499 | 0.569 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.651 |
DOC_USP7_UBL2_3 | 124 | 128 | PF12436 | 0.658 |
DOC_USP7_UBL2_3 | 386 | 390 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 209 | 218 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 22 | 26 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 345 | 354 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 447 | 457 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 480 | 490 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.575 |
LIG_BRCT_BRCA1_1 | 336 | 340 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 85 | 89 | PF00533 | 0.647 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.577 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.420 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.553 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.499 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.516 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.520 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.780 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.493 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.446 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.646 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.805 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.549 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.471 |
LIG_LIR_Apic_2 | 238 | 242 | PF02991 | 0.327 |
LIG_LIR_Apic_2 | 268 | 274 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 170 | 180 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 349 | 356 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 398 | 408 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 451 | 460 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 489 | 497 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 426 | 430 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 451 | 456 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.453 |
LIG_PCNA_yPIPBox_3 | 198 | 211 | PF02747 | 0.503 |
LIG_PDZ_Class_3 | 508 | 513 | PF00595 | 0.325 |
LIG_Pex14_2 | 85 | 89 | PF04695 | 0.647 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.367 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.440 |
LIG_SH2_CRK | 439 | 443 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 316 | 320 | PF00017 | 0.502 |
LIG_SH2_NCK_1 | 401 | 405 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 439 | 443 | PF00017 | 0.535 |
LIG_SH2_STAT3 | 507 | 510 | PF00017 | 0.464 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.404 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.672 |
LIG_TRAF2_1 | 322 | 325 | PF00917 | 0.605 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.535 |
LIG_TRAF2_1 | 489 | 492 | PF00917 | 0.453 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.603 |
LIG_TRAF2_2 | 470 | 475 | PF00917 | 0.492 |
LIG_TRFH_1 | 453 | 457 | PF08558 | 0.535 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.559 |
MOD_CDK_SPK_2 | 280 | 285 | PF00069 | 0.605 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.706 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.746 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.443 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.489 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.471 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.758 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.377 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.503 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.393 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.713 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.453 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.749 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.565 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.515 |
MOD_GlcNHglycan | 296 | 301 | PF01048 | 0.783 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.445 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.537 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.680 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.414 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.713 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.684 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.458 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.453 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.331 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.311 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.544 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.630 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.397 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.452 |
MOD_PKA_1 | 117 | 123 | PF00069 | 0.706 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.499 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.538 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.552 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.375 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.551 |
MOD_PKB_1 | 343 | 351 | PF00069 | 0.437 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.330 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.315 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.558 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.479 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.560 |
MOD_Plk_2-3 | 214 | 220 | PF00069 | 0.340 |
MOD_Plk_2-3 | 298 | 304 | PF00069 | 0.632 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.679 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.497 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.567 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.518 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.683 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.466 |
MOD_SUMO_for_1 | 266 | 269 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 4 | 11 | PF00179 | 0.437 |
TRG_DiLeu_BaEn_4 | 325 | 331 | PF01217 | 0.389 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.440 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.304 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGL8 | Leptomonas seymouri | 62% | 99% |
A0A1X0P4S2 | Trypanosomatidae | 40% | 100% |
A0A3Q8IQ93 | Leishmania donovani | 91% | 100% |
A0A3S5IQY8 | Trypanosoma rangeli | 38% | 99% |
A4HNG8 | Leishmania braziliensis | 74% | 100% |
A4IC59 | Leishmania infantum | 91% | 100% |
C9ZYE4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AFX9 | Leishmania major | 90% | 100% |
V5DQH4 | Trypanosoma cruzi | 43% | 100% |