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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 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:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HH35
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0032182 | ubiquitin-like protein binding | 3 | 1 |
GO:0043130 | ubiquitin binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 141 | 145 | PF00656 | 0.385 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.561 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.497 |
DEG_COP1_1 | 310 | 317 | PF00400 | 0.474 |
DEG_SPOP_SBC_1 | 265 | 269 | PF00917 | 0.686 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.516 |
DOC_CKS1_1 | 362 | 367 | PF01111 | 0.383 |
DOC_CKS1_1 | 89 | 94 | PF01111 | 0.615 |
DOC_MAPK_DCC_7 | 384 | 393 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 384 | 393 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 419 | 428 | PF00069 | 0.375 |
DOC_PP1_RVXF_1 | 119 | 125 | PF00149 | 0.299 |
DOC_PP2B_LxvP_1 | 67 | 70 | PF13499 | 0.517 |
DOC_PP2B_PxIxI_1 | 388 | 394 | PF00149 | 0.510 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.373 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.580 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 163 | 171 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 350 | 360 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 96 | 106 | PF00244 | 0.607 |
LIG_AP2alpha_2 | 244 | 246 | PF02296 | 0.672 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.541 |
LIG_BIR_III_4 | 256 | 260 | PF00653 | 0.520 |
LIG_deltaCOP1_diTrp_1 | 219 | 223 | PF00928 | 0.538 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.456 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.671 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.505 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.729 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.415 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.521 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.514 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.519 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.572 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.538 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 244 | 249 | PF02991 | 0.604 |
LIG_LIR_Apic_2 | 329 | 334 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 413 | 418 | PF02991 | 0.415 |
LIG_NRBOX | 372 | 378 | PF00104 | 0.376 |
LIG_PDZ_Class_2 | 425 | 430 | PF00595 | 0.509 |
LIG_SH2_CRK | 349 | 353 | PF00017 | 0.325 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.566 |
LIG_SH2_NCK_1 | 385 | 389 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 28 | 32 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.376 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.591 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.600 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.603 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.559 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.381 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.674 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.622 |
LIG_SUMO_SIM_par_1 | 138 | 144 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 310 | 316 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 324 | 330 | PF11976 | 0.360 |
MOD_CDK_SPK_2 | 44 | 49 | PF00069 | 0.479 |
MOD_CDK_SPxxK_3 | 361 | 368 | PF00069 | 0.498 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.453 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.707 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.529 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.578 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.502 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.425 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.526 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.658 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.650 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.720 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.762 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.421 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.582 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.604 |
MOD_DYRK1A_RPxSP_1 | 361 | 365 | PF00069 | 0.510 |
MOD_DYRK1A_RPxSP_1 | 88 | 92 | PF00069 | 0.684 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.522 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.324 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.522 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.727 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.617 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.582 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.463 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.697 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.665 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.474 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.428 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.715 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.421 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.632 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.495 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.544 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.633 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.380 |
MOD_PIKK_1 | 203 | 209 | PF00454 | 0.432 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.440 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.467 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.517 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.503 |
MOD_Plk_2-3 | 329 | 335 | PF00069 | 0.489 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.347 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.432 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.501 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.561 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.713 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.512 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.405 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.725 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.718 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.641 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.700 |
TRG_DiLeu_BaLyEn_6 | 211 | 216 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.379 |
TRG_ER_diArg_1 | 345 | 348 | PF00400 | 0.408 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T7 | Leptomonas seymouri | 57% | 100% |
A0A0S4JDU8 | Bodo saltans | 27% | 83% |
A0A1X0NZG7 | Trypanosomatidae | 27% | 97% |
A0A3Q8IH33 | Leishmania donovani | 83% | 100% |
A0A3R7M3Q4 | Trypanosoma rangeli | 27% | 100% |
A4I486 | Leishmania infantum | 83% | 100% |
C9ZKP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9ADN5 | Leishmania major | 83% | 100% |
E9AM45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
V5B4U5 | Trypanosoma cruzi | 27% | 100% |