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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0031464 | Cul4A-RING E3 ubiquitin ligase complex | 6 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0080008 | Cul4-RING E3 ubiquitin ligase complex | 5 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AMQ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 107 | 111 | PF00656 | 0.555 |
CLV_C14_Caspase3-7 | 226 | 230 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 317 | 321 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 432 | 436 | PF00656 | 0.558 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.539 |
CLV_PCSK_FUR_1 | 381 | 385 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.439 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.528 |
DEG_SCF_FBW7_2 | 97 | 103 | PF00400 | 0.625 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.572 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.632 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.698 |
DOC_ANK_TNKS_1 | 281 | 288 | PF00023 | 0.663 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.514 |
DOC_CKS1_1 | 97 | 102 | PF01111 | 0.552 |
DOC_MAPK_gen_1 | 393 | 399 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 81 | 88 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.542 |
DOC_MIT_MIM_1 | 389 | 398 | PF04212 | 0.401 |
DOC_PP1_RVXF_1 | 371 | 378 | PF00149 | 0.579 |
DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.691 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.448 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.792 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.710 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 393 | 398 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 456 | 462 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.723 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.685 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.553 |
LIG_EH1_1 | 365 | 373 | PF00400 | 0.597 |
LIG_EH1_1 | 415 | 423 | PF00400 | 0.486 |
LIG_eIF4E_1 | 366 | 372 | PF01652 | 0.521 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.504 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.558 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.500 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.393 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.715 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.399 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.493 |
LIG_PTAP_UEV_1 | 271 | 276 | PF05743 | 0.667 |
LIG_SH2_PTP2 | 423 | 426 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.424 |
LIG_SH3_1 | 423 | 429 | PF00018 | 0.572 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.577 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.664 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.608 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.572 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 21 | 27 | PF11976 | 0.494 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.668 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.517 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.395 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.552 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.631 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.598 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.792 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.628 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.630 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.567 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.384 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.535 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.315 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.669 |
MOD_DYRK1A_RPxSP_1 | 96 | 100 | PF00069 | 0.545 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.658 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.626 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.580 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.542 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.393 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.648 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.696 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.629 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.628 |
MOD_GlcNHglycan | 475 | 480 | PF01048 | 0.571 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.549 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.493 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.564 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.541 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.575 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.667 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.624 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.659 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.634 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.452 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.570 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.529 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.424 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.514 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.377 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.457 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.670 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.404 |
MOD_NEK2_2 | 90 | 95 | PF00069 | 0.524 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.629 |
MOD_PKA_1 | 393 | 399 | PF00069 | 0.449 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.755 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.476 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.553 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.648 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.470 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.456 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.576 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.692 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.598 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.458 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.418 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.521 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.399 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.791 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.567 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.628 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.710 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.505 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.527 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.710 |
TRG_DiLeu_BaLyEn_6 | 423 | 428 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 385 | 388 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U2 | Leptomonas seymouri | 39% | 100% |
A0A3S7WQQ0 | Leishmania donovani | 88% | 100% |
A4H5N4 | Leishmania braziliensis | 69% | 100% |
A4HTX8 | Leishmania infantum | 88% | 100% |
Q4QHW7 | Leishmania major | 88% | 100% |