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: A4HGL2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.575 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.482 |
DEG_APCC_DBOX_1 | 158 | 166 | PF00400 | 0.508 |
DEG_MDM2_SWIB_1 | 276 | 284 | PF02201 | 0.485 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.524 |
DOC_CDC14_PxL_1 | 241 | 249 | PF14671 | 0.419 |
DOC_CKS1_1 | 254 | 259 | PF01111 | 0.278 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.612 |
DOC_CYCLIN_RxL_1 | 243 | 251 | PF00134 | 0.535 |
DOC_MAPK_MEF2A_6 | 246 | 254 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 353 | 360 | PF00149 | 0.443 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.656 |
DOC_PP4_FxxP_1 | 254 | 257 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.364 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.629 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 253 | 258 | PF00397 | 0.201 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 246 | 251 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 88 | 92 | PF00244 | 0.558 |
LIG_APCC_ABBA_1 | 165 | 170 | PF00400 | 0.507 |
LIG_BIR_III_2 | 172 | 176 | PF00653 | 0.570 |
LIG_BIR_III_4 | 15 | 19 | PF00653 | 0.392 |
LIG_BRCT_BRCA1_1 | 250 | 254 | PF00533 | 0.487 |
LIG_deltaCOP1_diTrp_1 | 278 | 282 | PF00928 | 0.479 |
LIG_DLG_GKlike_1 | 246 | 253 | PF00625 | 0.424 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.466 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.488 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.323 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.513 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.426 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.579 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.526 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.508 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.573 |
LIG_LIR_Apic_2 | 251 | 257 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 286 | 297 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 275 | 279 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 286 | 292 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.432 |
LIG_MYND_1 | 239 | 243 | PF01753 | 0.227 |
LIG_Pex14_2 | 276 | 280 | PF04695 | 0.483 |
LIG_SH2_GRB2like | 75 | 78 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.443 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.633 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.585 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.573 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.644 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.544 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.520 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 34 | 41 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 246 | 251 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 374 | 379 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 414 | 419 | PF11976 | 0.564 |
LIG_TRFH_1 | 326 | 330 | PF08558 | 0.329 |
LIG_WRC_WIRS_1 | 273 | 278 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 279 | 284 | PF05994 | 0.484 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.480 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.750 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.528 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.529 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.598 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.564 |
MOD_DYRK1A_RPxSP_1 | 371 | 375 | PF00069 | 0.356 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.649 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.714 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.537 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.658 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.616 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.557 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.569 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.525 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.535 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.558 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.630 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.696 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.459 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.417 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.501 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.640 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.582 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.625 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.413 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.578 |
MOD_N-GLC_1 | 76 | 81 | PF02516 | 0.600 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.430 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.535 |
MOD_NEK2_2 | 163 | 168 | PF00069 | 0.288 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.447 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.502 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.502 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.598 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.568 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.400 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.424 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.502 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.443 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.459 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.541 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.567 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.456 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.547 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.559 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.389 |
MOD_ProDKin_1 | 253 | 259 | PF00069 | 0.197 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.750 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.576 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.331 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.613 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.548 |
TRG_DiLeu_BaEn_1 | 395 | 400 | PF01217 | 0.564 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 243 | 248 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P824 | Leptomonas seymouri | 54% | 100% |
A0A1X0NSF3 | Trypanosomatidae | 35% | 100% |
A0A3R7MSX4 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X1L8 | Leishmania donovani | 84% | 100% |
A4I3N8 | Leishmania infantum | 84% | 100% |
D0A8C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AZX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q8A6 | Leishmania major | 84% | 100% |
V5AVA5 | Trypanosoma cruzi | 39% | 100% |