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:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HD23
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 7 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.587 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.530 |
DEG_APCC_DBOX_1 | 61 | 69 | PF00400 | 0.443 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.499 |
DEG_SPOP_SBC_1 | 26 | 30 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.606 |
DOC_CYCLIN_RxL_1 | 103 | 110 | PF00134 | 0.479 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 257 | 266 | PF00134 | 0.521 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.597 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.543 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.482 |
LIG_14-3-3_CanoR_1 | 106 | 112 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 6 | 14 | PF00244 | 0.655 |
LIG_BIR_III_2 | 342 | 346 | PF00653 | 0.414 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_2 | 363 | 369 | PF00533 | 0.414 |
LIG_Clathr_ClatBox_1 | 289 | 293 | PF01394 | 0.447 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.631 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.304 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.469 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.688 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.600 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.515 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.469 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.514 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.529 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 283 | 292 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 364 | 372 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.414 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.521 |
LIG_SH3_1 | 182 | 188 | PF00018 | 0.514 |
LIG_SH3_2 | 185 | 190 | PF14604 | 0.521 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.615 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 214 | 220 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 27 | 38 | PF11976 | 0.641 |
LIG_SUMO_SIM_par_1 | 287 | 294 | PF11976 | 0.452 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.584 |
LIG_TRAF2_1 | 285 | 288 | PF00917 | 0.454 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.577 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.694 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.642 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.472 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.496 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.543 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.605 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.476 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.572 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.503 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.609 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.460 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.401 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.583 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.571 |
MOD_DYRK1A_RPxSP_1 | 66 | 70 | PF00069 | 0.477 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.605 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.627 |
MOD_GlcNHglycan | 330 | 335 | PF01048 | 0.305 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.570 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.516 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.759 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.648 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.460 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.425 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.516 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.447 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.663 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.490 |
MOD_N-GLC_1 | 361 | 366 | PF02516 | 0.321 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.549 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.482 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.468 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.409 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.421 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.396 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.632 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.457 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.661 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.516 |
MOD_PK_1 | 316 | 322 | PF00069 | 0.421 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.660 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.536 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.616 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.537 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.464 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.595 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.661 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.460 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.521 |
MOD_Plk_2-3 | 282 | 288 | PF00069 | 0.460 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.596 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.532 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.698 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.636 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.516 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.485 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.479 |
TRG_DiLeu_BaEn_2 | 174 | 180 | PF01217 | 0.650 |
TRG_DiLeu_BaEn_4 | 287 | 293 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.663 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.453 |
TRG_NES_CRM1_1 | 88 | 101 | PF08389 | 0.551 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.596 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS7 | Leptomonas seymouri | 41% | 100% |
A0A3Q8IBP7 | Leishmania donovani | 79% | 100% |
A4I0L0 | Leishmania infantum | 79% | 100% |
E9AWH1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QB00 | Leishmania major | 78% | 100% |