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 | yes | yes: 3, no: 2 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4H5U9
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.631 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.429 |
CLV_PCSK_FUR_1 | 311 | 315 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.429 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.310 |
CLV_PCSK_PC7_1 | 199 | 205 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.474 |
DEG_SPOP_SBC_1 | 263 | 267 | PF00917 | 0.621 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.412 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 144 | 155 | PF00134 | 0.593 |
DOC_CYCLIN_RxL_1 | 224 | 233 | PF00134 | 0.613 |
DOC_MAPK_gen_1 | 311 | 319 | PF00069 | 0.676 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.456 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.584 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 311 | 320 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 348 | 358 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 45 | 49 | PF00244 | 0.440 |
LIG_Actin_RPEL_3 | 123 | 142 | PF02755 | 0.457 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.589 |
LIG_BIR_III_4 | 173 | 177 | PF00653 | 0.474 |
LIG_EH_1 | 328 | 332 | PF12763 | 0.720 |
LIG_EH1_1 | 223 | 231 | PF00400 | 0.604 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.581 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.599 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.436 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.709 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.699 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.534 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.408 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.474 |
LIG_FHA_2 | 264 | 270 | PF00498 | 0.620 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.708 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.732 |
LIG_Integrin_isoDGR_2 | 349 | 351 | PF01839 | 0.457 |
LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.643 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.819 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.445 |
LIG_PCNA_PIPBox_1 | 125 | 134 | PF02747 | 0.457 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.754 |
LIG_SH2_CRK | 388 | 392 | PF00017 | 0.623 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.754 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.595 |
LIG_SH3_1 | 245 | 251 | PF00018 | 0.647 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.647 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.627 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.680 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.530 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.323 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.659 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.739 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.687 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.682 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.434 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.415 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.653 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.625 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.617 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.629 |
MOD_CK2_1 | 337 | 343 | PF00069 | 0.659 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.706 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.467 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.375 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.380 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.341 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.505 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.470 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.632 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.611 |
MOD_GlcNHglycan | 381 | 385 | PF01048 | 0.495 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.671 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.647 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.375 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.547 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.780 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.670 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.698 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.798 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.709 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.458 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.447 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.718 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.375 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.313 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.458 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.559 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.469 |
MOD_OFUCOSY | 83 | 90 | PF10250 | 0.666 |
MOD_PKA_1 | 313 | 319 | PF00069 | 0.635 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.503 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.754 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.749 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.646 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.416 |
MOD_PKB_1 | 311 | 319 | PF00069 | 0.632 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.680 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.288 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.253 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.458 |
MOD_Plk_4 | 44 | 50 | PF00069 | 0.450 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.525 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.733 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.736 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.656 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.479 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.613 |
MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.604 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.754 |
TRG_ENDOCYTIC_2 | 388 | 391 | PF00928 | 0.813 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.487 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 311 | 314 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.790 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQW1 | Leishmania donovani | 71% | 94% |
A4HU43 | Leishmania infantum | 72% | 94% |
E9AMX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 95% |
Q4QHQ4 | Leishmania major | 66% | 100% |