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: 30 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 43 |
NetGPI | no | yes: 0, no: 43 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4H3C7
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 44 |
GO:0006793 | phosphorus metabolic process | 3 | 44 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 44 |
GO:0006807 | nitrogen compound metabolic process | 2 | 44 |
GO:0008152 | metabolic process | 1 | 44 |
GO:0009987 | cellular process | 1 | 44 |
GO:0016310 | phosphorylation | 5 | 44 |
GO:0019538 | protein metabolic process | 3 | 44 |
GO:0036211 | protein modification process | 4 | 44 |
GO:0043170 | macromolecule metabolic process | 3 | 44 |
GO:0043412 | macromolecule modification | 4 | 44 |
GO:0044237 | cellular metabolic process | 2 | 44 |
GO:0044238 | primary metabolic process | 2 | 44 |
GO:0071704 | organic substance metabolic process | 2 | 44 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 44 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 44 |
GO:0003824 | catalytic activity | 1 | 44 |
GO:0004672 | protein kinase activity | 3 | 44 |
GO:0005488 | binding | 1 | 44 |
GO:0005524 | ATP binding | 5 | 44 |
GO:0016301 | kinase activity | 4 | 44 |
GO:0016740 | transferase activity | 2 | 44 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 44 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 44 |
GO:0017076 | purine nucleotide binding | 4 | 44 |
GO:0030554 | adenyl nucleotide binding | 5 | 44 |
GO:0032553 | ribonucleotide binding | 3 | 44 |
GO:0032555 | purine ribonucleotide binding | 4 | 44 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 44 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 44 |
GO:0036094 | small molecule binding | 2 | 44 |
GO:0043167 | ion binding | 2 | 44 |
GO:0043168 | anion binding | 3 | 44 |
GO:0097159 | organic cyclic compound binding | 2 | 44 |
GO:0097367 | carbohydrate derivative binding | 2 | 44 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 44 |
GO:1901265 | nucleoside phosphate binding | 3 | 44 |
GO:1901363 | heterocyclic compound binding | 2 | 44 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 25 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.461 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.282 |
CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.286 |
CLV_PCSK_PC7_1 | 443 | 449 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.299 |
DEG_APCC_DBOX_1 | 202 | 210 | PF00400 | 0.163 |
DEG_APCC_DBOX_1 | 442 | 450 | PF00400 | 0.266 |
DEG_APCC_DBOX_1 | 455 | 463 | PF00400 | 0.425 |
DEG_SPOP_SBC_1 | 119 | 123 | PF00917 | 0.445 |
DOC_CDC14_PxL_1 | 358 | 366 | PF14671 | 0.312 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.163 |
DOC_CYCLIN_RxL_1 | 386 | 397 | PF00134 | 0.197 |
DOC_CYCLIN_yCln2_LP_2 | 488 | 494 | PF00134 | 0.390 |
DOC_MAPK_gen_1 | 316 | 325 | PF00069 | 0.316 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.276 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.343 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.236 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 88 | 93 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 45 | 55 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.558 |
LIG_14-3-3_CterR_2 | 525 | 529 | PF00244 | 0.397 |
LIG_Actin_WH2_2 | 195 | 212 | PF00022 | 0.221 |
LIG_Actin_WH2_2 | 431 | 449 | PF00022 | 0.247 |
LIG_BIR_III_2 | 227 | 231 | PF00653 | 0.163 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 82 | 86 | PF00533 | 0.467 |
LIG_Clathr_ClatBox_1 | 435 | 439 | PF01394 | 0.384 |
LIG_deltaCOP1_diTrp_1 | 375 | 383 | PF00928 | 0.423 |
LIG_deltaCOP1_diTrp_1 | 6 | 10 | PF00928 | 0.636 |
LIG_eIF4E_1 | 359 | 365 | PF01652 | 0.337 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.427 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.474 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.319 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.378 |
LIG_HOMEOBOX | 5 | 8 | PF00046 | 0.486 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 236 | 244 | PF02991 | 0.291 |
LIG_LIR_Gen_1 | 294 | 304 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 3 | 10 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.636 |
LIG_Rb_pABgroove_1 | 220 | 228 | PF01858 | 0.343 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.358 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 461 | 464 | PF00017 | 0.226 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.254 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.578 |
LIG_SH2_STAT3 | 424 | 427 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.354 |
LIG_SH3_2 | 472 | 477 | PF14604 | 0.419 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.460 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.283 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.513 |
LIG_SUMO_SIM_par_1 | 433 | 439 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.395 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.373 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.458 |
LIG_TYR_ITIM | 459 | 464 | PF00017 | 0.227 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.263 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.287 |
MOD_CK1_1 | 306 | 312 | PF00069 | 0.343 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.346 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.248 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.470 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.640 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.715 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.510 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.585 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.287 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.700 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.640 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.515 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.667 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.413 |
MOD_GlcNHglycan | 170 | 175 | PF01048 | 0.234 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.258 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.585 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.324 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.653 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.616 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.682 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.703 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.780 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.200 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.480 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.361 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.316 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.374 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.289 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.538 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.600 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.603 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.729 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.536 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.473 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.334 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.311 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.291 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.233 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.270 |
MOD_NEK2_2 | 303 | 308 | PF00069 | 0.328 |
MOD_PIKK_1 | 14 | 20 | PF00454 | 0.460 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.195 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.297 |
MOD_PKA_2 | 442 | 448 | PF00069 | 0.323 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.654 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.293 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.377 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.345 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.316 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.263 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.372 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.480 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.236 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.388 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.306 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.364 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.618 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.541 |
MOD_ProDKin_1 | 88 | 94 | PF00069 | 0.701 |
TRG_DiLeu_BaEn_1 | 400 | 405 | PF01217 | 0.195 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.342 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.299 |
TRG_NES_CRM1_1 | 328 | 342 | PF08389 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 490 | 495 | PF00026 | 0.471 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2D3 | Leptomonas seymouri | 50% | 100% |
A0A0S4J6L4 | Bodo saltans | 26% | 100% |
A0A0S4J757 | Bodo saltans | 27% | 98% |
A0A0S4JIJ6 | Bodo saltans | 26% | 94% |
A0A0S4JMY6 | Bodo saltans | 25% | 69% |
A0A1X0NIA0 | Trypanosomatidae | 33% | 100% |
A0A1X0NKA1 | Trypanosomatidae | 38% | 100% |
A0A1X0NNF5 | Trypanosomatidae | 29% | 85% |
A0A1X0P9C4 | Trypanosomatidae | 32% | 100% |
A0A2I0BVG8 | Plasmodium falciparum (isolate NF54) | 23% | 100% |
A0A3Q8IAQ1 | Leishmania donovani | 32% | 100% |
A0A3Q8IFK8 | Leishmania donovani | 28% | 100% |
A0A3Q8IFW0 | Leishmania donovani | 32% | 100% |
A0A3Q8IIG1 | Leishmania donovani | 29% | 100% |
A0A3Q8IPJ5 | Leishmania donovani | 26% | 100% |
A0A3R7KRP1 | Trypanosoma rangeli | 27% | 100% |
A0A3R7KZ44 | Trypanosoma rangeli | 29% | 90% |
A0A3R7RC77 | Trypanosoma rangeli | 25% | 90% |
A0A3S5H4Z4 | Leishmania donovani | 77% | 100% |
A0A3S7WWE7 | Leishmania donovani | 28% | 100% |
A0A3S7X6T8 | Leishmania donovani | 27% | 100% |
A0A3S7X7Y2 | Leishmania donovani | 26% | 100% |
A0A422N3U8 | Trypanosoma rangeli | 25% | 73% |
A0A422N3Y6 | Trypanosoma rangeli | 24% | 100% |
A0A422NUF0 | Trypanosoma rangeli | 27% | 100% |
A4HAS1 | Leishmania braziliensis | 26% | 100% |
A4HBL4 | Leishmania braziliensis | 28% | 100% |
A4HCE6 | Leishmania braziliensis | 32% | 100% |
A4HFA1 | Leishmania braziliensis | 26% | 100% |
A4HH03 | Leishmania braziliensis | 30% | 100% |
A4HJT5 | Leishmania braziliensis | 29% | 100% |
A4HJW2 | Leishmania braziliensis | 32% | 100% |
A4HLR0 | Leishmania braziliensis | 28% | 100% |
A4HRM6 | Leishmania infantum | 77% | 100% |
A4HZA2 | Leishmania infantum | 28% | 100% |
A4HZW8 | Leishmania infantum | 32% | 100% |
A4I2H8 | Leishmania infantum | 27% | 100% |
A4I435 | Leishmania infantum | 30% | 100% |
A4I7A1 | Leishmania infantum | 28% | 100% |
A4I7C4 | Leishmania infantum | 32% | 100% |
A4I960 | Leishmania infantum | 27% | 100% |
A4I9Y5 | Leishmania infantum | 26% | 100% |
C9ZIZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZWI1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACA4 | Leishmania major | 76% | 100% |
E9AJJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 98% |
E9AUY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AVS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9AYN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B0C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B2B7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B436 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B4Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
P05772 | Oryctolagus cuniculus | 22% | 79% |
P62343 | Plasmodium falciparum (isolate K1 / Thailand) | 23% | 100% |
P62344 | Plasmodium falciparum (isolate 3D7) | 23% | 100% |
P68403 | Rattus norvegicus | 22% | 79% |
P68404 | Mus musculus | 22% | 79% |
Q07832 | Mus musculus | 26% | 88% |
Q08942 | Trypanosoma brucei brucei | 27% | 100% |
Q13177 | Homo sapiens | 26% | 100% |
Q17941 | Caenorhabditis elegans | 24% | 98% |
Q4P5N0 | Ustilago maydis (strain 521 / FGSC 9021) | 23% | 71% |
Q4Q2Z2 | Leishmania major | 25% | 100% |
Q4Q3Y9 | Leishmania major | 27% | 100% |
Q4Q5T9 | Leishmania major | 32% | 100% |
Q4Q5W2 | Leishmania major | 29% | 100% |
Q4Q7W2 | Leishmania major | 30% | 100% |
Q4Q8T4 | Leishmania major | 27% | 100% |
Q4QBQ2 | Leishmania major | 33% | 100% |
Q4QCK0 | Leishmania major | 27% | 100% |
Q5VQQ5 | Oryza sativa subsp. japonica | 26% | 100% |
Q64303 | Rattus norvegicus | 27% | 100% |
Q6Z2M9 | Oryza sativa subsp. japonica | 27% | 100% |
Q8CIN4 | Mus musculus | 27% | 100% |
V5BSA6 | Trypanosoma cruzi | 27% | 81% |