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: A4HIN7
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 | 255 | 259 | PF00656 | 0.219 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.546 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.129 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.240 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.440 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.474 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.504 |
DOC_CKS1_1 | 444 | 449 | PF01111 | 0.377 |
DOC_MAPK_gen_1 | 400 | 407 | PF00069 | 0.505 |
DOC_PP2B_LxvP_1 | 435 | 438 | PF13499 | 0.355 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.304 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 234 | 240 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 245 | 254 | PF00244 | 0.246 |
LIG_14-3-3_CanoR_1 | 267 | 276 | PF00244 | 0.222 |
LIG_14-3-3_CanoR_1 | 401 | 406 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.440 |
LIG_BRCT_BRCA1_1 | 297 | 301 | PF00533 | 0.336 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.409 |
LIG_EH1_1 | 285 | 293 | PF00400 | 0.349 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.167 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.123 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.255 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.316 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.474 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.305 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.291 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.209 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 298 | 304 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 47 | 54 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.213 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 326 | 331 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.213 |
LIG_MAD2 | 52 | 60 | PF02301 | 0.465 |
LIG_NBox_RRM_1 | 138 | 148 | PF00076 | 0.308 |
LIG_PCNA_yPIPBox_3 | 377 | 390 | PF02747 | 0.351 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.377 |
LIG_Rb_pABgroove_1 | 96 | 104 | PF01858 | 0.351 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.269 |
LIG_SH2_NCK_1 | 22 | 26 | PF00017 | 0.286 |
LIG_SH2_NCK_1 | 273 | 277 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.286 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.419 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.266 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.334 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.453 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.413 |
LIG_SH3_3 | 409 | 415 | PF00018 | 0.424 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.205 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.207 |
LIG_SUMO_SIM_par_1 | 353 | 359 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 93 | 99 | PF11976 | 0.259 |
LIG_UBA3_1 | 69 | 74 | PF00899 | 0.322 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.377 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.322 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.440 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.214 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.477 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.565 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.586 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.635 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.287 |
MOD_GlcNHglycan | 189 | 193 | PF01048 | 0.564 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.411 |
MOD_GlcNHglycan | 346 | 350 | PF01048 | 0.422 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.244 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.593 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.427 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.425 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.485 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.254 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.262 |
MOD_LATS_1 | 243 | 249 | PF00433 | 0.291 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.763 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.144 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.138 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.447 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.384 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.515 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.632 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.262 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.285 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.433 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.243 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.478 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.391 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.453 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.341 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.616 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.271 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.291 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.387 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.255 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.349 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.668 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.322 |
MOD_SUMO_rev_2 | 223 | 229 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.322 |
TRG_DiLeu_BaEn_2 | 390 | 396 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.257 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M9 | Leptomonas seymouri | 25% | 100% |
A0A0N1I470 | Leptomonas seymouri | 70% | 88% |
A0A0N1PDI6 | Leptomonas seymouri | 22% | 75% |
A0A0S4IPA6 | Bodo saltans | 43% | 100% |
A0A0S4IPI7 | Bodo saltans | 28% | 90% |
A0A0S4JSF9 | Bodo saltans | 23% | 84% |
A0A1X0NRR8 | Trypanosomatidae | 21% | 100% |
A0A1X0P1F1 | Trypanosomatidae | 48% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 25% | 80% |
A0A3Q8IC75 | Leishmania donovani | 80% | 90% |
A0A3Q8IL77 | Leishmania donovani | 23% | 74% |
A0A3Q8ITK0 | Leishmania donovani | 25% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 46% | 100% |
A0A3R7M693 | Trypanosoma rangeli | 23% | 67% |
A0A422NS01 | Trypanosoma rangeli | 23% | 80% |
A0A422NYJ0 | Trypanosoma rangeli | 23% | 97% |
A4H9B8 | Leishmania braziliensis | 25% | 70% |
A4HAY2 | Leishmania braziliensis | 22% | 76% |
A4HKU5 | Leishmania braziliensis | 26% | 100% |
A4I5Y4 | Leishmania infantum | 80% | 90% |
A4I8C4 | Leishmania infantum | 25% | 100% |
A4IA41 | Leishmania infantum | 23% | 74% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 80% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 90% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 74% |
Q4Q2T0 | Leishmania major | 23% | 74% |
Q4Q4X2 | Leishmania major | 24% | 100% |
Q4Q6Y7 | Leishmania major | 82% | 100% |
Q4V3C7 | Arabidopsis thaliana | 32% | 91% |
Q67XQ0 | Arabidopsis thaliana | 32% | 91% |
Q8RY60 | Arabidopsis thaliana | 30% | 86% |
Q8VZI2 | Arabidopsis thaliana | 30% | 100% |
Q9LTD8 | Arabidopsis thaliana | 29% | 90% |
Q9USJ3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 66% |
Q9ZQR4 | Arabidopsis thaliana | 31% | 100% |
Q9ZVS8 | Arabidopsis thaliana | 33% | 90% |
V5BEH2 | Trypanosoma cruzi | 23% | 66% |
V5BKR5 | Trypanosoma cruzi | 24% | 78% |
V5DM70 | Trypanosoma cruzi | 24% | 100% |
V5DNW3 | Trypanosoma cruzi | 48% | 100% |