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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HE93
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.724 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.761 |
DEG_APCC_DBOX_1 | 316 | 324 | PF00400 | 0.519 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.421 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.532 |
DOC_CKS1_1 | 27 | 32 | PF01111 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 323 | 326 | PF00134 | 0.462 |
DOC_MAPK_MEF2A_6 | 222 | 231 | PF00069 | 0.488 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.500 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 270 | 274 | PF12436 | 0.761 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 26 | 31 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 111 | 118 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 192 | 200 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 261 | 269 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 327 | 335 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 308 | 324 | PF00022 | 0.588 |
LIG_Actin_WH2_2 | 403 | 420 | PF00022 | 0.568 |
LIG_Actin_WH2_2 | 72 | 90 | PF00022 | 0.381 |
LIG_Clathr_ClatBox_1 | 81 | 85 | PF01394 | 0.365 |
LIG_CtBP_PxDLS_1 | 40 | 44 | PF00389 | 0.493 |
LIG_DLG_GKlike_1 | 413 | 421 | PF00625 | 0.465 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.345 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.540 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.446 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.492 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.304 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.380 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.503 |
LIG_GBD_Chelix_1 | 79 | 87 | PF00786 | 0.368 |
LIG_LIR_Gen_1 | 146 | 154 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.481 |
LIG_MYND_1 | 37 | 41 | PF01753 | 0.488 |
LIG_PDZ_Class_3 | 431 | 436 | PF00595 | 0.654 |
LIG_Pex14_1 | 118 | 122 | PF04695 | 0.414 |
LIG_RPA_C_Fungi | 408 | 420 | PF08784 | 0.307 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.288 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.480 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.661 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.492 |
LIG_SUMO_SIM_anti_2 | 78 | 85 | PF11976 | 0.362 |
LIG_SUMO_SIM_par_1 | 159 | 164 | PF11976 | 0.338 |
LIG_SUMO_SIM_par_1 | 225 | 230 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 371 | 377 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 78 | 85 | PF11976 | 0.362 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.306 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.568 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.505 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.313 |
LIG_TYR_ITIM | 121 | 126 | PF00017 | 0.283 |
LIG_UBA3_1 | 372 | 378 | PF00899 | 0.444 |
LIG_WW_1 | 325 | 328 | PF00397 | 0.516 |
LIG_WW_3 | 324 | 328 | PF00397 | 0.506 |
MOD_CDK_SPxxK_3 | 41 | 48 | PF00069 | 0.494 |
MOD_CDK_SPxxK_3 | 91 | 98 | PF00069 | 0.405 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.423 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.620 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.668 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.569 |
MOD_CK1_1 | 89 | 95 | PF00069 | 0.532 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.477 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.505 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.580 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.686 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.544 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.720 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.498 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.758 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.787 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.555 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.510 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.578 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.689 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.681 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.515 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.701 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.638 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.494 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.651 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.565 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.554 |
MOD_LATS_1 | 191 | 197 | PF00433 | 0.517 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.801 |
MOD_N-GLC_2 | 242 | 244 | PF02516 | 0.654 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.493 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.383 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.530 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.494 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.563 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.510 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.413 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.487 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.510 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.680 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.478 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.512 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.715 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.549 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.803 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.554 |
MOD_ProDKin_1 | 26 | 32 | PF00069 | 0.479 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.505 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.449 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.413 |
MOD_SUMO_rev_2 | 246 | 252 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 264 | 272 | PF00179 | 0.755 |
TRG_DiLeu_BaEn_1 | 281 | 286 | PF01217 | 0.801 |
TRG_DiLeu_BaEn_1 | 316 | 321 | PF01217 | 0.556 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.566 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 153 | 167 | PF08389 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I869 | Leptomonas seymouri | 44% | 100% |
A0A3Q8IFE5 | Leishmania donovani | 67% | 100% |
A4I1N9 | Leishmania infantum | 67% | 100% |
C9ZK88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AXS3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 66% | 100% |
Q4Q9P8 | Leishmania major | 66% | 96% |
V5BHX9 | Trypanosoma cruzi | 25% | 100% |