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 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HU43
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 | 355 | 359 | PF00656 | 0.766 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.581 |
CLV_PCSK_FUR_1 | 362 | 366 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 364 | 366 | PF00082 | 0.543 |
CLV_PCSK_PC7_1 | 148 | 154 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.700 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.551 |
DOC_CYCLIN_RxL_1 | 144 | 155 | PF00134 | 0.674 |
DOC_CYCLIN_RxL_1 | 224 | 234 | PF00134 | 0.678 |
DOC_MAPK_gen_1 | 18 | 28 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.747 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 21 | 29 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.567 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.662 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.748 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.833 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 323 | 332 | PF00244 | 0.811 |
LIG_Actin_RPEL_3 | 123 | 142 | PF02755 | 0.571 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BIR_III_2 | 69 | 73 | PF00653 | 0.417 |
LIG_EH_1 | 340 | 344 | PF12763 | 0.795 |
LIG_EH1_1 | 223 | 231 | PF00400 | 0.671 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.651 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.664 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.752 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.806 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.746 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.564 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.585 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.826 |
LIG_LIR_Gen_1 | 20 | 30 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 345 | 352 | PF02991 | 0.760 |
LIG_LIR_Gen_1 | 412 | 419 | PF02991 | 0.694 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 345 | 350 | PF02991 | 0.786 |
LIG_LIR_Nem_3 | 412 | 418 | PF02991 | 0.738 |
LIG_PCNA_PIPBox_1 | 125 | 134 | PF02747 | 0.573 |
LIG_Pex14_2 | 23 | 27 | PF04695 | 0.412 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.808 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.551 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.808 |
LIG_SH2_PTP2 | 415 | 418 | PF00017 | 0.701 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.635 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.661 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.701 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.552 |
LIG_SH3_3 | 383 | 389 | PF00018 | 0.807 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.579 |
LIG_SUMO_SIM_anti_2 | 113 | 118 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.399 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.762 |
LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.771 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.723 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.750 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.703 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.677 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.587 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.702 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.516 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.597 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.491 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.700 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.483 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.705 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.500 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.385 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.533 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.549 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.508 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.784 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.548 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.640 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.807 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.796 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.761 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.680 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.593 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.485 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.671 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.610 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.720 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.610 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.533 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.830 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.591 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.516 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.687 |
MOD_N-GLC_2 | 303 | 305 | PF02516 | 0.600 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.483 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.327 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.593 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.581 |
MOD_OFUCOSY | 83 | 90 | PF10250 | 0.672 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.599 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.742 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.769 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.485 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.679 |
MOD_Plk_2-3 | 289 | 295 | PF00069 | 0.612 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.388 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.309 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.327 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.614 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.483 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.743 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.807 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.630 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.692 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.622 |
MOD_SUMO_rev_2 | 64 | 73 | PF00179 | 0.617 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.772 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.681 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.773 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.734 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQW1 | Leishmania donovani | 99% | 100% |
A4H5U9 | Leishmania braziliensis | 72% | 100% |
E9AMX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q4QHQ4 | Leishmania major | 91% | 100% |