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: E9AMX2
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 | 352 | 356 | PF00656 | 0.754 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.537 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.389 |
CLV_PCSK_PC7_1 | 148 | 154 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.316 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.500 |
DOC_CYCLIN_RxL_1 | 144 | 155 | PF00134 | 0.623 |
DOC_CYCLIN_RxL_1 | 224 | 234 | PF00134 | 0.619 |
DOC_MAPK_gen_1 | 18 | 28 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 21 | 29 | PF00069 | 0.418 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.487 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.679 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.830 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 315 | 322 | PF00244 | 0.728 |
LIG_Actin_RPEL_3 | 123 | 142 | PF02755 | 0.489 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.615 |
LIG_CtBP_PxDLS_1 | 249 | 253 | PF00389 | 0.609 |
LIG_EH_1 | 337 | 341 | PF12763 | 0.742 |
LIG_EH1_1 | 223 | 231 | PF00400 | 0.609 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.605 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.467 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.757 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.500 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.489 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.734 |
LIG_LIR_Gen_1 | 25 | 35 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 342 | 349 | PF02991 | 0.722 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 342 | 347 | PF02991 | 0.720 |
LIG_PCNA_PIPBox_1 | 125 | 134 | PF02747 | 0.489 |
LIG_PTAP_UEV_1 | 1 | 6 | PF05743 | 0.484 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.758 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.758 |
LIG_SH2_PTP2 | 412 | 415 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.609 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.511 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.770 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.531 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.344 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.704 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.749 |
LIG_WW_3 | 320 | 324 | PF00397 | 0.531 |
MOD_CDK_SPxxK_3 | 368 | 375 | PF00069 | 0.653 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.789 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.559 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.609 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.514 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.801 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.657 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.356 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.645 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.405 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.335 |
MOD_GlcNHglycan | 234 | 239 | PF01048 | 0.594 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.564 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.491 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.602 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.668 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.645 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.726 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.692 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.681 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.405 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.583 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.624 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.575 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.745 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.630 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.605 |
MOD_N-GLC_2 | 301 | 303 | PF02516 | 0.549 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.450 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.429 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.568 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.498 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.483 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.631 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.653 |
MOD_NEK2_2 | 322 | 327 | PF00069 | 0.605 |
MOD_OFUCOSY | 83 | 90 | PF10250 | 0.602 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.533 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.662 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.704 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.612 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.551 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.545 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.619 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.571 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.322 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.334 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.262 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.403 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.572 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.405 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.800 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.699 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.574 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.621 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.541 |
MOD_SUMO_rev_2 | 161 | 171 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 64 | 73 | PF00179 | 0.571 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.774 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQW1 | Leishmania donovani | 84% | 99% |
A4H5U9 | Leishmania braziliensis | 66% | 94% |
A4HU43 | Leishmania infantum | 84% | 99% |
Q4QHQ4 | Leishmania major | 82% | 100% |