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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0016020 | membrane | 2 | 5 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4I492
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.702 |
CLV_C14_Caspase3-7 | 289 | 293 | PF00656 | 0.714 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.726 |
CLV_C14_Caspase3-7 | 91 | 95 | PF00656 | 0.634 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.470 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.394 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.571 |
DOC_CYCLIN_RxL_1 | 99 | 109 | PF00134 | 0.598 |
DOC_MAPK_MEF2A_6 | 347 | 354 | PF00069 | 0.716 |
DOC_MAPK_MEF2A_6 | 58 | 65 | PF00069 | 0.584 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 218 | 227 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.702 |
LIG_APCC_ABBAyCdc20_2 | 358 | 364 | PF00400 | 0.622 |
LIG_deltaCOP1_diTrp_1 | 302 | 309 | PF00928 | 0.676 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.603 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.595 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.687 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.622 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.674 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.576 |
LIG_FHA_2 | 287 | 293 | PF00498 | 0.818 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.730 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.515 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 303 | 310 | PF02991 | 0.675 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.646 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.676 |
LIG_NRBOX | 75 | 81 | PF00104 | 0.564 |
LIG_PDZ_Class_2 | 443 | 448 | PF00595 | 0.650 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.315 |
LIG_SH2_NCK_1 | 164 | 168 | PF00017 | 0.395 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.610 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.717 |
LIG_Sin3_3 | 25 | 32 | PF02671 | 0.641 |
LIG_SUMO_SIM_anti_2 | 10 | 18 | PF11976 | 0.669 |
LIG_SUMO_SIM_anti_2 | 351 | 356 | PF11976 | 0.722 |
LIG_SUMO_SIM_par_1 | 316 | 324 | PF11976 | 0.699 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.628 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.653 |
LIG_TRAF2_1 | 375 | 378 | PF00917 | 0.684 |
LIG_TRAF2_1 | 426 | 429 | PF00917 | 0.600 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.644 |
MOD_CDK_SPxK_1 | 225 | 231 | PF00069 | 0.604 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.671 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.601 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.659 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.268 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.702 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.755 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.658 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.613 |
MOD_CK2_1 | 240 | 246 | PF00069 | 0.622 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.697 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.765 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.729 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.531 |
MOD_DYRK1A_RPxSP_1 | 311 | 315 | PF00069 | 0.680 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.414 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.587 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.490 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.402 |
MOD_GlcNHglycan | 322 | 326 | PF01048 | 0.485 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.522 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.607 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.486 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.446 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.459 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.633 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.592 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.603 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.477 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.315 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.797 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.692 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.627 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.688 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.710 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.678 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.674 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.608 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.722 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.596 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.605 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.315 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.717 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.723 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.652 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.623 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.649 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.575 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.671 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.640 |
MOD_PKA_1 | 357 | 363 | PF00069 | 0.667 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.643 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.572 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.671 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.568 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.315 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.448 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.244 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.604 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.675 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.667 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.708 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 322 | 330 | PF00179 | 0.702 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.644 |
TRG_DiLeu_LyEn_5 | 59 | 64 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 157 | 160 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.666 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.401 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7G2 | Leptomonas seymouri | 62% | 100% |
A0A3S7X253 | Leishmania donovani | 100% | 100% |
A4HH48 | Leishmania braziliensis | 74% | 98% |
E9ADP8 | Leishmania major | 94% | 100% |
E9AM32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |