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: 15 |
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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9ACA4
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 24 |
GO:0006793 | phosphorus metabolic process | 3 | 24 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 24 |
GO:0006807 | nitrogen compound metabolic process | 2 | 24 |
GO:0008152 | metabolic process | 1 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0016310 | phosphorylation | 5 | 24 |
GO:0019538 | protein metabolic process | 3 | 24 |
GO:0036211 | protein modification process | 4 | 24 |
GO:0043170 | macromolecule metabolic process | 3 | 24 |
GO:0043412 | macromolecule modification | 4 | 24 |
GO:0044237 | cellular metabolic process | 2 | 24 |
GO:0044238 | primary metabolic process | 2 | 24 |
GO:0071704 | organic substance metabolic process | 2 | 24 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 24 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 24 |
GO:0003824 | catalytic activity | 1 | 24 |
GO:0004672 | protein kinase activity | 3 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0016301 | kinase activity | 4 | 24 |
GO:0016740 | transferase activity | 2 | 24 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 24 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 24 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.211 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.266 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.264 |
CLV_PCSK_PC7_1 | 444 | 450 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.267 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.305 |
DEG_APCC_DBOX_1 | 456 | 464 | PF00400 | 0.338 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.498 |
DEG_SIAH_1 | 73 | 81 | PF03145 | 0.476 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.247 |
DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.467 |
DOC_ANK_TNKS_1 | 491 | 498 | PF00023 | 0.394 |
DOC_CDC14_PxL_1 | 359 | 367 | PF14671 | 0.307 |
DOC_CYCLIN_RxL_1 | 387 | 398 | PF00134 | 0.230 |
DOC_MAPK_gen_1 | 317 | 326 | PF00069 | 0.328 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.640 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.288 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 492 | 499 | PF00244 | 0.596 |
LIG_14-3-3_CterR_2 | 526 | 530 | PF00244 | 0.514 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.286 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.648 |
LIG_deltaCOP1_diTrp_1 | 376 | 384 | PF00928 | 0.311 |
LIG_deltaCOP1_diTrp_1 | 6 | 10 | PF00928 | 0.599 |
LIG_eIF4E_1 | 360 | 366 | PF01652 | 0.243 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.535 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.433 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.304 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.298 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.733 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.311 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.311 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.656 |
LIG_HOMEOBOX | 5 | 8 | PF00046 | 0.516 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.619 |
LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 496 | 507 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 310 | 315 | PF02991 | 0.220 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 459 | 465 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 496 | 502 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.463 |
LIG_Rb_pABgroove_1 | 221 | 229 | PF01858 | 0.311 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.311 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.294 |
LIG_SH2_PTP2 | 462 | 465 | PF00017 | 0.243 |
LIG_SH2_SRC | 222 | 225 | PF00017 | 0.256 |
LIG_SH2_SRC | 462 | 465 | PF00017 | 0.275 |
LIG_SH2_STAP1 | 425 | 429 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.260 |
LIG_SH2_STAT3 | 128 | 131 | PF00017 | 0.497 |
LIG_SH2_STAT3 | 425 | 428 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.328 |
LIG_SH3_3 | 229 | 235 | PF00018 | 0.471 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.248 |
LIG_SUMO_SIM_par_1 | 463 | 469 | PF11976 | 0.360 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.227 |
LIG_TYR_ITIM | 460 | 465 | PF00017 | 0.242 |
LIG_WW_1 | 231 | 234 | PF00397 | 0.211 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.463 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.333 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.347 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.311 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.432 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.237 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.374 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.697 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.640 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.541 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.367 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.387 |
MOD_Cter_Amidation | 254 | 257 | PF01082 | 0.211 |
MOD_GlcNHglycan | 12 | 17 | PF01048 | 0.747 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.671 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.454 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.400 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.403 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.645 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.346 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.454 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.710 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.243 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.372 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.487 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.252 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.382 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.757 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.645 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.261 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.545 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.613 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.297 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.455 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.425 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.372 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.312 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.250 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.361 |
MOD_NEK2_2 | 162 | 167 | PF00069 | 0.257 |
MOD_NEK2_2 | 293 | 298 | PF00069 | 0.387 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.257 |
MOD_NEK2_2 | 94 | 99 | PF00069 | 0.525 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.227 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.674 |
MOD_PIKK_1 | 510 | 516 | PF00454 | 0.310 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.450 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.324 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.328 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.695 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.492 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.323 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.319 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.389 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.326 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.231 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.364 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.314 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.288 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.321 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.317 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.602 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.553 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.654 |
TRG_DiLeu_BaEn_1 | 401 | 406 | PF01217 | 0.227 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.243 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.313 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.277 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 447 | 449 | PF00400 | 0.262 |
TRG_NES_CRM1_1 | 329 | 343 | PF08389 | 0.227 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2D3 | Leptomonas seymouri | 52% | 100% |
A0A0N1I9A0 | Leptomonas seymouri | 27% | 82% |
A0A0S4IX86 | Bodo saltans | 29% | 100% |
A0A0S4J757 | Bodo saltans | 26% | 98% |
A0A0S4JCI5 | Bodo saltans | 27% | 83% |
A0A0S4JIJ6 | Bodo saltans | 26% | 94% |
A0A0S4JMY6 | Bodo saltans | 24% | 69% |
A0A1X0NFW4 | Trypanosomatidae | 28% | 100% |
A0A1X0NKA1 | Trypanosomatidae | 38% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 33% | 100% |
A0A3Q8IDY1 | Leishmania donovani | 28% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 29% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 32% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 29% | 100% |
A0A3Q8IPJ5 | Leishmania donovani | 26% | 100% |
A0A3S5H4Z4 | Leishmania donovani | 94% | 100% |
A0A3S5H789 | Leishmania donovani | 27% | 100% |
A0A3S7WWE7 | Leishmania donovani | 28% | 100% |
A0A3S7X6T8 | Leishmania donovani | 28% | 100% |
A0A422N8E7 | Trypanosoma rangeli | 27% | 68% |
A0A422NT89 | Trypanosoma rangeli | 23% | 81% |
A4H3C7 | Leishmania braziliensis | 76% | 100% |
A4HBL4 | Leishmania braziliensis | 27% | 100% |
A4HCE6 | Leishmania braziliensis | 32% | 100% |
A4HFA1 | Leishmania braziliensis | 26% | 100% |
A4HHP8 | Leishmania braziliensis | 28% | 100% |
A4HJT5 | Leishmania braziliensis | 28% | 100% |
A4HJW2 | Leishmania braziliensis | 32% | 100% |
A4HLR0 | Leishmania braziliensis | 28% | 100% |
A4HRM6 | Leishmania infantum | 94% | 100% |
A4HW76 | Leishmania infantum | 25% | 66% |
A4HYX6 | Leishmania infantum | 27% | 100% |
A4HZA2 | Leishmania infantum | 28% | 100% |
A4HZW8 | Leishmania infantum | 33% | 100% |
A4I2H8 | Leishmania infantum | 26% | 100% |
A4I435 | Leishmania infantum | 29% | 100% |
A4I4W3 | Leishmania infantum | 28% | 100% |
A4I7A1 | Leishmania infantum | 29% | 100% |
A4I7C4 | Leishmania infantum | 32% | 100% |
A4I960 | Leishmania infantum | 28% | 100% |
C9ZIZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZQL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 83% |
E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
E9AUY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AYN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
F4JBP3 | Arabidopsis thaliana | 28% | 75% |
P0C8M8 | Zea mays | 25% | 85% |
P22209 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 100% |
P31748 | AKT8 murine leukemia virus | 24% | 100% |
P31750 | Mus musculus | 24% | 100% |
P34101 | Dictyostelium discoideum | 23% | 89% |
P38147 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |
P47196 | Rattus norvegicus | 24% | 100% |
Q01314 | Bos taurus | 24% | 100% |
Q06850 | Arabidopsis thaliana | 27% | 87% |
Q07832 | Mus musculus | 27% | 88% |
Q38870 | Arabidopsis thaliana | 25% | 82% |
Q4Q3Y9 | Leishmania major | 28% | 100% |
Q4Q5T9 | Leishmania major | 32% | 100% |
Q4Q5W2 | Leishmania major | 29% | 100% |
Q4Q7W2 | Leishmania major | 29% | 100% |
Q4Q8T4 | Leishmania major | 26% | 100% |
Q4QBQ2 | Leishmania major | 34% | 100% |
Q4QCK0 | Leishmania major | 27% | 100% |
Q5KQF5 | Oryza sativa subsp. japonica | 29% | 100% |
Q6Z2M9 | Oryza sativa subsp. japonica | 27% | 100% |
Q9Y6E0 | Homo sapiens | 26% | 100% |
Q9ZV15 | Arabidopsis thaliana | 26% | 91% |
V5BHW8 | Trypanosoma cruzi | 25% | 84% |
V5BLW4 | Trypanosoma cruzi | 31% | 69% |