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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q6Y7
Term | Name | Level | Count |
---|---|---|---|
GO:0010960 | magnesium ion homeostasis | 8 | 11 |
GO:0042592 | homeostatic process | 3 | 11 |
GO:0048878 | chemical homeostasis | 4 | 11 |
GO:0050801 | monoatomic ion homeostasis | 5 | 11 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 11 |
GO:0055080 | monoatomic cation homeostasis | 6 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0065008 | regulation of biological quality | 2 | 11 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 11 |
GO:0098771 | inorganic ion homeostasis | 6 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.472 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.136 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.314 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.289 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.489 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.561 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.538 |
DOC_ANK_TNKS_1 | 413 | 420 | PF00023 | 0.391 |
DOC_MAPK_gen_1 | 287 | 295 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 384 | 392 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 403 | 410 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 287 | 295 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 403 | 410 | PF00069 | 0.498 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.376 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.410 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 323 | 331 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.489 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.437 |
LIG_BRCT_BRCA1_1 | 31 | 35 | PF00533 | 0.430 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.458 |
LIG_EH1_1 | 288 | 296 | PF00400 | 0.373 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.204 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.125 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.321 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.338 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.356 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.482 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.517 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.370 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.562 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.341 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.297 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.414 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.538 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.328 |
LIG_LIR_Apic_2 | 301 | 307 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 273 | 283 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 332 | 341 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 47 | 54 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.262 |
LIG_MAD2 | 162 | 170 | PF02301 | 0.278 |
LIG_MAD2 | 52 | 60 | PF02301 | 0.510 |
LIG_NBox_RRM_1 | 138 | 148 | PF00076 | 0.456 |
LIG_PCNA_yPIPBox_3 | 384 | 393 | PF02747 | 0.372 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.423 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.297 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.417 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.309 |
LIG_SH2_SRC | 348 | 351 | PF00017 | 0.370 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.330 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.335 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.374 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.497 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.264 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.266 |
LIG_SUMO_SIM_par_1 | 292 | 298 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 388 | 394 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 406 | 413 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 93 | 100 | PF11976 | 0.327 |
LIG_TYR_ITSM | 272 | 279 | PF00017 | 0.462 |
LIG_UBA3_1 | 69 | 74 | PF00899 | 0.384 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.384 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.461 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.492 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.214 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.515 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.497 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.639 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.733 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.500 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.596 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.559 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.354 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.761 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.398 |
MOD_GlcNHglycan | 349 | 353 | PF01048 | 0.546 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.580 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.311 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.483 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.475 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.522 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.384 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.719 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.331 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.751 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.168 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.440 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.682 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.157 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.494 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.442 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.577 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.331 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.353 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.352 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.486 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.482 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.530 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.492 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.419 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.602 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.398 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.701 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.585 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.355 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.675 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.358 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.718 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.460 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.373 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.371 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.332 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.404 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.410 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.688 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.384 |
MOD_SUMO_rev_2 | 226 | 232 | PF00179 | 0.547 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_3 | 189 | 195 | PF01217 | 0.631 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M9 | Leptomonas seymouri | 26% | 99% |
A0A0N1I470 | Leptomonas seymouri | 71% | 82% |
A0A0N1PDI6 | Leptomonas seymouri | 24% | 70% |
A0A0S4IPA6 | Bodo saltans | 42% | 100% |
A0A0S4IPI7 | Bodo saltans | 28% | 84% |
A0A0S4JSF9 | Bodo saltans | 25% | 78% |
A0A1X0NRR8 | Trypanosomatidae | 22% | 96% |
A0A1X0P1F1 | Trypanosomatidae | 48% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 26% | 74% |
A0A3Q8IC75 | Leishmania donovani | 97% | 84% |
A0A3Q8IL77 | Leishmania donovani | 24% | 69% |
A0A3Q8ITK0 | Leishmania donovani | 24% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 46% | 100% |
A0A422NS01 | Trypanosoma rangeli | 24% | 74% |
A0A422NYJ0 | Trypanosoma rangeli | 25% | 90% |
A4HAY2 | Leishmania braziliensis | 24% | 71% |
A4HIN7 | Leishmania braziliensis | 82% | 93% |
A4I5Y4 | Leishmania infantum | 97% | 84% |
A4I8C4 | Leishmania infantum | 25% | 100% |
A4IA41 | Leishmania infantum | 24% | 69% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 75% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 84% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 69% |
Q17586 | Caenorhabditis elegans | 24% | 90% |
Q4Q2T0 | Leishmania major | 24% | 69% |
Q4V3C7 | Arabidopsis thaliana | 32% | 85% |
Q67XQ0 | Arabidopsis thaliana | 32% | 85% |
Q8RY60 | Arabidopsis thaliana | 30% | 80% |
Q8VZI2 | Arabidopsis thaliana | 28% | 99% |
Q9LTD8 | Arabidopsis thaliana | 27% | 84% |
Q9ZQR4 | Arabidopsis thaliana | 28% | 99% |
Q9ZVS8 | Arabidopsis thaliana | 34% | 84% |
V5BKR5 | Trypanosoma cruzi | 24% | 73% |
V5DM70 | Trypanosoma cruzi | 25% | 93% |
V5DNW3 | Trypanosoma cruzi | 47% | 100% |