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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZX9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 157 | 165 | PF00400 | 0.499 |
DEG_MDM2_SWIB_1 | 275 | 283 | PF02201 | 0.483 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.518 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.599 |
DOC_CYCLIN_RxL_1 | 242 | 250 | PF00134 | 0.532 |
DOC_MAPK_gen_1 | 157 | 166 | PF00069 | 0.287 |
DOC_MAPK_HePTP_8 | 4 | 16 | PF00069 | 0.259 |
DOC_MAPK_MEF2A_6 | 160 | 168 | PF00069 | 0.266 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.259 |
DOC_PP1_RVXF_1 | 354 | 361 | PF00149 | 0.429 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.611 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.423 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.522 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.760 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.542 |
LIG_14-3-3_CanoR_1 | 245 | 250 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 330 | 338 | PF00244 | 0.578 |
LIG_APCC_ABBA_1 | 164 | 169 | PF00400 | 0.503 |
LIG_BIR_III_2 | 122 | 126 | PF00653 | 0.674 |
LIG_BIR_III_2 | 171 | 175 | PF00653 | 0.576 |
LIG_BRCT_BRCA1_1 | 249 | 253 | PF00533 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 277 | 281 | PF00928 | 0.477 |
LIG_DLG_GKlike_1 | 245 | 252 | PF00625 | 0.420 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.495 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.311 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.484 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.401 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.578 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.517 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.493 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.759 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.602 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.433 |
LIG_Pex14_2 | 275 | 279 | PF04695 | 0.476 |
LIG_SH2_GRB2like | 74 | 77 | PF00017 | 0.603 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.314 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.591 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.572 |
LIG_SH3_3 | 312 | 318 | PF00018 | 0.582 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.626 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.541 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.508 |
LIG_SH3_3 | 94 | 100 | PF00018 | 0.554 |
LIG_SH3_CIN85_PxpxPR_1 | 240 | 245 | PF14604 | 0.389 |
LIG_SUMO_SIM_anti_2 | 248 | 253 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 26 | 40 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 245 | 250 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 415 | 420 | PF11976 | 0.560 |
LIG_TRAF2_1 | 301 | 304 | PF00917 | 0.703 |
LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.624 |
LIG_WRC_WIRS_1 | 272 | 277 | PF05994 | 0.498 |
MOD_CDK_SPK_2 | 59 | 64 | PF00069 | 0.524 |
MOD_CDK_SPxxK_3 | 238 | 245 | PF00069 | 0.480 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.402 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.582 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.657 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.580 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.751 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.577 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.672 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.636 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.587 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.644 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.560 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.509 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.525 |
MOD_GlcNHglycan | 57 | 61 | PF01048 | 0.599 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.528 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.574 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.459 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.417 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.484 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.585 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.552 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.596 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.404 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.568 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.588 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.425 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.528 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.532 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.660 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.447 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.602 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.577 |
MOD_Plk_2-3 | 271 | 277 | PF00069 | 0.415 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.495 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.438 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.457 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.537 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.475 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.575 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.554 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.389 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.765 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.549 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.310 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.598 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.657 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.539 |
TRG_DiLeu_BaEn_1 | 396 | 401 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_1 | 65 | 70 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.507 |
TRG_ER_diArg_1 | 4 | 7 | PF00400 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P824 | Leptomonas seymouri | 52% | 100% |
A0A1X0NSF3 | Trypanosomatidae | 34% | 100% |
A0A3R7MSX4 | Trypanosoma rangeli | 39% | 100% |
A0A3S7X1L8 | Leishmania donovani | 92% | 100% |
A4HGL2 | Leishmania braziliensis | 84% | 100% |
A4I3N8 | Leishmania infantum | 92% | 100% |
D0A8C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
Q4Q8A6 | Leishmania major | 91% | 100% |
V5AVA5 | Trypanosoma cruzi | 37% | 100% |