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: E9B177
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_NRD_NRD_1 | 289 | 291 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.608 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.131 |
CLV_Separin_Metazoa | 322 | 326 | PF03568 | 0.269 |
DEG_APCC_DBOX_1 | 172 | 180 | PF00400 | 0.242 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.442 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.476 |
DEG_SPOP_SBC_1 | 470 | 474 | PF00917 | 0.347 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.506 |
DOC_CKS1_1 | 374 | 379 | PF01111 | 0.290 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 386 | 394 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 405 | 412 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 289 | 297 | PF00069 | 0.365 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.472 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.370 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.442 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.338 |
LIG_Clathr_ClatBox_1 | 43 | 47 | PF01394 | 0.411 |
LIG_CtBP_PxDLS_1 | 409 | 413 | PF00389 | 0.333 |
LIG_EH1_1 | 290 | 298 | PF00400 | 0.342 |
LIG_EVH1_2 | 456 | 460 | PF00568 | 0.362 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.169 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.125 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.257 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.311 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.475 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.509 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.517 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.535 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.307 |
LIG_FHA_2 | 191 | 197 | PF00498 | 0.534 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.401 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.297 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.254 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.450 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.409 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.506 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.292 |
LIG_LIR_Apic_2 | 303 | 309 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 275 | 285 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 334 | 343 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 47 | 54 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 99 | 110 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 331 | 336 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.215 |
LIG_MAD2 | 52 | 60 | PF02301 | 0.467 |
LIG_NBox_RRM_1 | 138 | 148 | PF00076 | 0.310 |
LIG_PCNA_yPIPBox_3 | 386 | 395 | PF02747 | 0.327 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.379 |
LIG_Rb_pABgroove_1 | 96 | 104 | PF01858 | 0.353 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.262 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.262 |
LIG_SH2_SRC | 350 | 353 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.420 |
LIG_SH3_2 | 309 | 314 | PF14604 | 0.247 |
LIG_SH3_2 | 453 | 458 | PF14604 | 0.365 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.268 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.334 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.438 |
LIG_SH3_3 | 450 | 456 | PF00018 | 0.396 |
LIG_SH3_CIN85_PxpxPR_1 | 309 | 314 | PF14604 | 0.239 |
LIG_SH3_CIN85_PxpxPR_1 | 453 | 458 | PF14604 | 0.412 |
LIG_SUMO_SIM_anti_2 | 68 | 74 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 79 | 85 | PF11976 | 0.207 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.209 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.286 |
LIG_SUMO_SIM_par_1 | 358 | 364 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 390 | 396 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 408 | 415 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 93 | 100 | PF11976 | 0.261 |
LIG_TYR_ITSM | 274 | 281 | PF00017 | 0.351 |
LIG_UBA3_1 | 69 | 74 | PF00899 | 0.324 |
LIG_WW_3 | 311 | 315 | PF00397 | 0.271 |
LIG_WW_3 | 455 | 459 | PF00397 | 0.456 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.379 |
MOD_CDK_SPxxK_3 | 451 | 458 | PF00069 | 0.532 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.324 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.381 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.632 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.433 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.211 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.567 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.476 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.416 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.550 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.756 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.672 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.696 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.512 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.442 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.551 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.529 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.706 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.289 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.745 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.319 |
MOD_GlcNHglycan | 351 | 355 | PF01048 | 0.526 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.705 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.542 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.246 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.428 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.415 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.483 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.321 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.728 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.572 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.630 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.264 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.764 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.146 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.387 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.569 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.140 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.447 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.385 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.516 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.600 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.501 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.492 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.264 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.287 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.287 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.386 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.434 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.458 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.492 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.436 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.361 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.343 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.651 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.438 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.513 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.340 |
MOD_Plk_2-3 | 190 | 196 | PF00069 | 0.563 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.293 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.672 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.390 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.311 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.324 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.292 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.623 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.351 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.359 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.533 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.672 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.673 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.324 |
MOD_SUMO_rev_2 | 228 | 234 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 479 | 488 | PF00179 | 0.539 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.324 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1M9 | Leptomonas seymouri | 26% | 100% |
A0A0N1I470 | Leptomonas seymouri | 66% | 98% |
A0A0N1PDI6 | Leptomonas seymouri | 24% | 83% |
A0A0S4IPA6 | Bodo saltans | 40% | 100% |
A0A0S4JSF9 | Bodo saltans | 22% | 93% |
A0A1X0NRR8 | Trypanosomatidae | 24% | 100% |
A0A1X0P1F1 | Trypanosomatidae | 48% | 100% |
A0A1X0PAL3 | Trypanosomatidae | 26% | 89% |
A0A3Q8IC75 | Leishmania donovani | 91% | 100% |
A0A3Q8IL77 | Leishmania donovani | 25% | 82% |
A0A3Q8ITK0 | Leishmania donovani | 26% | 100% |
A0A3R7LBY6 | Trypanosoma rangeli | 45% | 100% |
A0A422NS01 | Trypanosoma rangeli | 24% | 89% |
A4HAY2 | Leishmania braziliensis | 23% | 85% |
A4HIN7 | Leishmania braziliensis | 78% | 99% |
A4HKU5 | Leishmania braziliensis | 25% | 100% |
A4I5Y4 | Leishmania infantum | 91% | 100% |
A4I8C4 | Leishmania infantum | 27% | 100% |
A4IA41 | Leishmania infantum | 25% | 82% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 89% |
D0A017 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 68% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 82% |
Q12296 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 71% |
Q4Q2T0 | Leishmania major | 25% | 82% |
Q4Q4X2 | Leishmania major | 26% | 100% |
Q4Q6Y7 | Leishmania major | 93% | 100% |
Q4V3C7 | Arabidopsis thaliana | 31% | 100% |
Q67XQ0 | Arabidopsis thaliana | 31% | 100% |
Q8RY60 | Arabidopsis thaliana | 29% | 95% |
Q8VZI2 | Arabidopsis thaliana | 28% | 100% |
Q9LTD8 | Arabidopsis thaliana | 28% | 100% |
Q9USJ3 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 74% |
V5BKR5 | Trypanosoma cruzi | 25% | 87% |
V5DM70 | Trypanosoma cruzi | 25% | 100% |
V5DNW3 | Trypanosoma cruzi | 47% | 100% |