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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 11 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: Q4Q8U0
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 13 |
GO:0006793 | phosphorus metabolic process | 3 | 13 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0016310 | phosphorylation | 5 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0036211 | protein modification process | 4 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043412 | macromolecule modification | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004672 | protein kinase activity | 3 | 13 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 11 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0016301 | kinase activity | 4 | 13 |
GO:0016740 | transferase activity | 2 | 13 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 13 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.316 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 162 | 164 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 60 | 62 | PF00082 | 0.427 |
CLV_PCSK_PC7_1 | 25 | 31 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.369 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.327 |
DEG_APCC_DBOX_1 | 207 | 215 | PF00400 | 0.426 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.571 |
DEG_APCC_KENBOX_2 | 404 | 408 | PF00400 | 0.447 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.426 |
DOC_CKS1_1 | 462 | 467 | PF01111 | 0.641 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.636 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.538 |
DOC_MAPK_gen_1 | 265 | 274 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 65 | 76 | PF00069 | 0.252 |
DOC_MAPK_MEF2A_6 | 208 | 215 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 69 | 76 | PF00069 | 0.374 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.447 |
DOC_USP7_UBL2_3 | 167 | 171 | PF12436 | 0.301 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 354 | 359 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 475 | 479 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.552 |
LIG_APCC_ABBAyCdc20_2 | 260 | 266 | PF00400 | 0.298 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 354 | 358 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_2 | 354 | 360 | PF00533 | 0.447 |
LIG_EH_1 | 406 | 410 | PF12763 | 0.369 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.679 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.515 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.335 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.395 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.458 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.458 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.447 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.637 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.445 |
LIG_LIR_Apic_2 | 275 | 281 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 305 | 311 | PF02991 | 0.298 |
LIG_LIR_Apic_2 | 97 | 101 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 355 | 365 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 400 | 409 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 400 | 404 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 438 | 442 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.479 |
LIG_MAD2 | 188 | 196 | PF02301 | 0.427 |
LIG_PDZ_Class_2 | 476 | 481 | PF00595 | 0.693 |
LIG_Pex14_1 | 468 | 472 | PF04695 | 0.660 |
LIG_Pex14_2 | 147 | 151 | PF04695 | 0.409 |
LIG_Pex14_2 | 31 | 35 | PF04695 | 0.367 |
LIG_Pex14_2 | 76 | 80 | PF04695 | 0.528 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.491 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.393 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 126 | 130 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.393 |
LIG_SH2_NCK_1 | 393 | 397 | PF00017 | 0.447 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 59 | 62 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.558 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.447 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.727 |
LIG_SUMO_SIM_anti_2 | 209 | 216 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 209 | 216 | PF11976 | 0.314 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.369 |
LIG_TRAF2_2 | 395 | 400 | PF00917 | 0.447 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.312 |
LIG_UBA3_1 | 165 | 171 | PF00899 | 0.447 |
LIG_WRC_WIRS_1 | 133 | 138 | PF05994 | 0.429 |
MOD_CDK_SPK_2 | 97 | 102 | PF00069 | 0.543 |
MOD_CDK_SPxK_1 | 461 | 467 | PF00069 | 0.667 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.435 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.341 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.528 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.605 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.480 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.427 |
MOD_Cter_Amidation | 23 | 26 | PF01082 | 0.426 |
MOD_Cter_Amidation | 27 | 30 | PF01082 | 0.426 |
MOD_GlcNHglycan | 154 | 159 | PF01048 | 0.433 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.389 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.426 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.345 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.315 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.659 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.426 |
MOD_N-GLC_2 | 68 | 70 | PF02516 | 0.312 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.409 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.369 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.367 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.396 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.557 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.426 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.415 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.426 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.670 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.582 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.422 |
MOD_Plk_2-3 | 438 | 444 | PF00069 | 0.692 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.482 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.379 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.298 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.415 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.426 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.599 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.637 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.518 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.552 |
MOD_SUMO_for_1 | 151 | 154 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 15 | 20 | PF00179 | 0.214 |
MOD_SUMO_rev_2 | 154 | 164 | PF00179 | 0.369 |
TRG_DiLeu_BaEn_1 | 455 | 460 | PF01217 | 0.724 |
TRG_DiLeu_BaLyEn_6 | 424 | 429 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 353 | 356 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 69 | 72 | PF00400 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 427 | 431 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N5 | Leptomonas seymouri | 28% | 100% |
A0A0N0P7K3 | Leptomonas seymouri | 66% | 100% |
A0A0N1IHM7 | Leptomonas seymouri | 27% | 82% |
A0A0S4IQ75 | Bodo saltans | 25% | 95% |
A0A0S4J842 | Bodo saltans | 24% | 90% |
A0A0S4JH92 | Bodo saltans | 39% | 97% |
A0A0S4JN19 | Bodo saltans | 27% | 78% |
A0A0S4JPZ7 | Bodo saltans | 26% | 100% |
A0A0S4JQP0 | Bodo saltans | 43% | 98% |
A0A0S4KKJ1 | Bodo saltans | 24% | 76% |
A0A0S4KMV7 | Bodo saltans | 27% | 100% |
A0A1X0P5U3 | Trypanosomatidae | 24% | 94% |
A0A1X0P834 | Trypanosomatidae | 45% | 100% |
A0A3Q8IHA5 | Leishmania donovani | 96% | 100% |
A0A3R7MPF2 | Trypanosoma rangeli | 25% | 74% |
A0A3S5H5G0 | Leishmania donovani | 27% | 100% |
A0A422N3U8 | Trypanosoma rangeli | 27% | 67% |
A0A422P3P9 | Trypanosoma rangeli | 48% | 97% |
A4H459 | Leishmania braziliensis | 28% | 100% |
A4H8C4 | Leishmania braziliensis | 29% | 100% |
A4HCE6 | Leishmania braziliensis | 25% | 100% |
A4HF96 | Leishmania braziliensis | 90% | 99% |
A4HSE2 | Leishmania infantum | 27% | 100% |
A4I2I8 | Leishmania infantum | 97% | 100% |
C0LGL9 | Arabidopsis thaliana | 29% | 82% |
C9ZLF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 76% |
C9ZPX9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZQP5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
C9ZUU2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 73% |
C9ZWL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 75% |
C9ZX15 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 96% |
E9AKB7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AYN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 99% |
E9B296 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
O14305 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
O96017 | Homo sapiens | 28% | 89% |
P28867 | Mus musculus | 25% | 71% |
P33886 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 80% |
P34947 | Homo sapiens | 28% | 82% |
Q0VD22 | Bos taurus | 29% | 99% |
Q4Q5T9 | Leishmania major | 28% | 100% |
Q4QJJ0 | Leishmania major | 26% | 100% |
Q60823 | Mus musculus | 27% | 100% |
Q6IP76 | Xenopus laevis | 26% | 99% |
Q9CAH1 | Arabidopsis thaliana | 27% | 100% |
Q9FZ36 | Arabidopsis thaliana | 24% | 74% |
Q9SN43 | Arabidopsis thaliana | 27% | 98% |
Q9ZSA2 | Arabidopsis thaliana | 27% | 91% |
V5BC57 | Trypanosoma cruzi | 47% | 97% |
V5BHW8 | Trypanosoma cruzi | 26% | 76% |
V5BL06 | Trypanosoma cruzi | 27% | 74% |
V5C234 | Trypanosoma cruzi | 26% | 88% |
V5D579 | Trypanosoma cruzi | 25% | 100% |