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: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AQD2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.706 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.354 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.328 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.588 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.562 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 161 | 167 | PF00149 | 0.389 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.278 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.359 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 126 | 131 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 186 | 190 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 21 | 27 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 332 | 340 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.337 |
LIG_14-3-3_CanoR_1 | 90 | 99 | PF00244 | 0.277 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.402 |
LIG_CaM_IQ_9 | 306 | 322 | PF13499 | 0.342 |
LIG_deltaCOP1_diTrp_1 | 242 | 246 | PF00928 | 0.281 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.524 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.450 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.525 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.510 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.477 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.427 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.411 |
LIG_LIR_Apic_2 | 68 | 73 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 261 | 272 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 376 | 385 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 94 | 104 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.287 |
LIG_NRBOX | 54 | 60 | PF00104 | 0.169 |
LIG_Pex14_1 | 190 | 194 | PF04695 | 0.314 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.315 |
LIG_Pex14_2 | 66 | 70 | PF04695 | 0.277 |
LIG_REV1ctd_RIR_1 | 128 | 136 | PF16727 | 0.312 |
LIG_SH2_CRK | 194 | 198 | PF00017 | 0.536 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.446 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.451 |
LIG_SH2_PTP2 | 23 | 26 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.441 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.298 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.401 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.582 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.687 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 341 | 351 | PF11976 | 0.415 |
LIG_TRAF2_1 | 139 | 142 | PF00917 | 0.337 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.407 |
LIG_TYR_ITIM | 192 | 197 | PF00017 | 0.351 |
LIG_TYR_ITSM | 206 | 213 | PF00017 | 0.341 |
LIG_WW_1 | 75 | 78 | PF00397 | 0.317 |
MOD_CDC14_SPxK_1 | 123 | 126 | PF00782 | 0.276 |
MOD_CDK_SPK_2 | 181 | 186 | PF00069 | 0.424 |
MOD_CDK_SPxK_1 | 120 | 126 | PF00069 | 0.276 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.312 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.396 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.424 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.496 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.358 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.379 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.533 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.492 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.410 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.553 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.673 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.532 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.328 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.560 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.455 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.487 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.493 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.317 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.460 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.372 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.477 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.320 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.439 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.450 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.337 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.360 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.516 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.438 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.436 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.438 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.562 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.579 |
TRG_AP2beta_CARGO_1 | 261 | 271 | PF09066 | 0.284 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.364 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 195 | 200 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 249 | 254 | PF00026 | 0.237 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7L5 | Leptomonas seymouri | 71% | 100% |
A0A0S4JE30 | Bodo saltans | 35% | 100% |
A0A0S4JK16 | Bodo saltans | 55% | 93% |
A0A1X0NVQ6 | Trypanosomatidae | 63% | 100% |
A0A1X0P1X9 | Trypanosomatidae | 34% | 100% |
A0A3Q8IFT0 | Leishmania donovani | 29% | 98% |
A0A3R7KWZ0 | Trypanosoma rangeli | 63% | 100% |
A0A3R7KYN0 | Trypanosoma rangeli | 32% | 100% |
A0A3S7WTN3 | Leishmania donovani | 92% | 100% |
A4H8A5 | Leishmania braziliensis | 87% | 100% |
A4HIA2 | Leishmania braziliensis | 28% | 91% |
A4HWM5 | Leishmania infantum | 93% | 100% |
A4I5I6 | Leishmania infantum | 29% | 98% |
C9ZXR2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9B0T1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 98% |
Q4Q7E7 | Leishmania major | 28% | 100% |
Q4QF43 | Leishmania major | 92% | 100% |
V5BPI9 | Trypanosoma cruzi | 34% | 100% |
V5BUE5 | Trypanosoma cruzi | 61% | 100% |