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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWH1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 8 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.616 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.598 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.490 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.615 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 254 | 263 | PF00134 | 0.516 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.472 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.609 |
DOC_USP7_UBL2_3 | 354 | 358 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.663 |
LIG_Clathr_ClatBox_1 | 286 | 290 | PF01394 | 0.438 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.611 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.351 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.465 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.616 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.612 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.506 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.476 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.504 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.460 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.503 |
LIG_LIR_Gen_1 | 135 | 144 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.445 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.621 |
LIG_SH2_STAP1 | 283 | 287 | PF00017 | 0.440 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.666 |
LIG_SUMO_SIM_anti_2 | 212 | 218 | PF11976 | 0.574 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.604 |
LIG_SUMO_SIM_par_1 | 284 | 291 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 30 | 38 | PF11976 | 0.715 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.812 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.597 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.441 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.561 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.745 |
MOD_CDK_SPxxK_3 | 222 | 229 | PF00069 | 0.635 |
MOD_CDK_SPxxK_3 | 66 | 73 | PF00069 | 0.457 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.652 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.462 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.571 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.616 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.450 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.621 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.659 |
MOD_DYRK1A_RPxSP_1 | 66 | 70 | PF00069 | 0.520 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.649 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.610 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.562 |
MOD_GlcNHglycan | 327 | 332 | PF01048 | 0.335 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.257 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.244 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.572 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.648 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.703 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.637 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.518 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.504 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.562 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.655 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.512 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.286 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.609 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.471 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.465 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.397 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.620 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.440 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.650 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.649 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.535 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.568 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.661 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.532 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.487 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.507 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.647 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.654 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.450 |
MOD_Plk_2-3 | 279 | 285 | PF00069 | 0.450 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.594 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.744 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.629 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.632 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.504 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.463 |
TRG_DiLeu_BaEn_2 | 173 | 179 | PF01217 | 0.632 |
TRG_DiLeu_BaEn_4 | 147 | 153 | PF01217 | 0.627 |
TRG_DiLeu_BaEn_4 | 284 | 290 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 215 | 220 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.441 |
TRG_NES_CRM1_1 | 88 | 101 | PF08389 | 0.542 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS7 | Leptomonas seymouri | 46% | 100% |
A0A3Q8IBP7 | Leishmania donovani | 93% | 100% |
A4HD23 | Leishmania braziliensis | 78% | 100% |
A4I0L0 | Leishmania infantum | 94% | 100% |
C9ZVI2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4QB00 | Leishmania major | 91% | 100% |