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: 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: Q4QHQ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.725 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.549 |
CLV_PCSK_FUR_1 | 365 | 369 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.332 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.368 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 367 | 369 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.370 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.505 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.413 |
DOC_CKS1_1 | 51 | 56 | PF01111 | 0.487 |
DOC_CYCLIN_RxL_1 | 144 | 155 | PF00134 | 0.596 |
DOC_CYCLIN_RxL_1 | 224 | 234 | PF00134 | 0.607 |
DOC_MAPK_gen_1 | 146 | 152 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 128 | 135 | PF00149 | 0.468 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.589 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.764 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 18 | 26 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.707 |
LIG_Actin_RPEL_3 | 123 | 142 | PF02755 | 0.467 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_EH_1 | 343 | 347 | PF12763 | 0.742 |
LIG_EH1_1 | 21 | 29 | PF00400 | 0.254 |
LIG_EH1_1 | 223 | 231 | PF00400 | 0.600 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.584 |
LIG_eIF4E_1 | 224 | 230 | PF01652 | 0.595 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.485 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.747 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.710 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.487 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.562 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.749 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.256 |
LIG_LIR_Gen_1 | 348 | 355 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 416 | 423 | PF02991 | 0.644 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 416 | 422 | PF02991 | 0.747 |
LIG_NRBOX | 22 | 28 | PF00104 | 0.254 |
LIG_PCNA_PIPBox_1 | 125 | 134 | PF02747 | 0.467 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.750 |
LIG_SH2_CRK | 51 | 55 | PF00017 | 0.501 |
LIG_SH2_NCK_1 | 350 | 354 | PF00017 | 0.750 |
LIG_SH2_PTP2 | 419 | 422 | PF00017 | 0.641 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.492 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.762 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 25 | 31 | PF11976 | 0.368 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.725 |
LIG_TRAF2_1 | 400 | 403 | PF00917 | 0.733 |
MOD_CDK_SPK_2 | 324 | 329 | PF00069 | 0.666 |
MOD_CDK_SPxxK_3 | 374 | 381 | PF00069 | 0.725 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.750 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.687 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.698 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.669 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.708 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.711 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.742 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.661 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.685 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.581 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.732 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.484 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.506 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.348 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.412 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.501 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.441 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.557 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.368 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.497 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.548 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.585 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.690 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.385 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.750 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.675 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.726 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.656 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.738 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.701 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.838 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.436 |
MOD_N-GLC_1 | 91 | 96 | PF02516 | 0.675 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.449 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.434 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.359 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.337 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.684 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.680 |
MOD_NEK2_2 | 328 | 333 | PF00069 | 0.688 |
MOD_OFUCOSY | 83 | 90 | PF10250 | 0.668 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.532 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.754 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.799 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.550 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.648 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.299 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.294 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.256 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.345 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.634 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.412 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.532 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.764 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.689 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.755 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.716 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.622 |
MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 64 | 73 | PF00179 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.553 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.750 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.586 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 346 | 349 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 380 | 382 | PF00400 | 0.731 |
TRG_Pf-PMV_PEXEL_1 | 161 | 165 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 203 | 207 | PF00026 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQW1 | Leishmania donovani | 91% | 100% |
A4H5U9 | Leishmania braziliensis | 66% | 100% |
A4HU43 | Leishmania infantum | 91% | 100% |
E9AMX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |