Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 1 |
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. | yes | yes: 20 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005829 | cytosol | 2 | 1 |
Related structures:
AlphaFold database: E9AP13
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0010181 | FMN binding | 4 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 1 |
GO:0016657 | oxidoreductase activity, acting on NAD(P)H, nitrogenous group as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.321 |
CLV_NRD_NRD_1 | 266 | 268 | PF00675 | 0.311 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.339 |
DEG_COP1_1 | 37 | 44 | PF00400 | 0.523 |
DOC_CYCLIN_RxL_1 | 214 | 224 | PF00134 | 0.552 |
DOC_MAPK_gen_1 | 232 | 239 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 267 | 274 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 232 | 239 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 53 | 60 | PF00069 | 0.552 |
DOC_MAPK_NFAT4_5 | 53 | 61 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 265 | 272 | PF00149 | 0.552 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.340 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.658 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 111 | 115 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 258 | 266 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 53 | 57 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 223 | 240 | PF00022 | 0.469 |
LIG_Actin_WH2_2 | 253 | 269 | PF00022 | 0.446 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.497 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.469 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.564 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.567 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.613 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.422 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.448 |
LIG_IRF3_LxIS_1 | 235 | 240 | PF10401 | 0.486 |
LIG_LIR_Apic_2 | 361 | 367 | PF02991 | 0.322 |
LIG_LIR_Gen_1 | 361 | 367 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 278 | 282 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.513 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 70 | 74 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.411 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.610 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.556 |
LIG_TRAF2_1 | 290 | 293 | PF00917 | 0.596 |
LIG_UBA3_1 | 219 | 228 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.523 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.485 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.613 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.433 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.194 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.283 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.578 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.323 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.618 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.272 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.497 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.520 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.486 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.480 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.537 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.490 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.479 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.598 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.523 |
MOD_PKA_1 | 89 | 95 | PF00069 | 0.552 |
MOD_PKA_2 | 110 | 116 | PF00069 | 0.558 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.512 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.469 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.542 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 215 | 218 | PF00400 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2A2 | Leptomonas seymouri | 68% | 100% |
A0A0N0P2S0 | Leptomonas seymouri | 32% | 100% |
A0A0N1HZB3 | Leptomonas seymouri | 39% | 68% |
A0A0S4IVY9 | Bodo saltans | 34% | 100% |
A0A0S4IYW9 | Bodo saltans | 40% | 100% |
A0A0S4JST7 | Bodo saltans | 28% | 68% |
A0A1D8PPK1 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 33% | 94% |
A0A1U8QTA2 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 39% | 99% |
A0A1X0P653 | Trypanosomatidae | 48% | 100% |
A0A3Q8ICQ9 | Leishmania donovani | 88% | 100% |
A0A422NKC3 | Trypanosoma rangeli | 46% | 100% |
A0A482NAR8 | Talaromyces variabilis | 29% | 95% |
A2TBU0 | Epichloe festucae var. lolii | 35% | 100% |
A4H6Z3 | Leishmania braziliensis | 80% | 100% |
A4IQK7 | Geobacillus thermodenitrificans (strain NG80-2) | 31% | 100% |
A8C7R3 | Claviceps fusiformis | 32% | 100% |
B8N8Q9 | Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / IAM 13836 / NRRL 3357 / JCM 12722 / SRRC 167) | 30% | 93% |
B8NWW6 | Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / IAM 13836 / NRRL 3357 / JCM 12722 / SRRC 167) | 37% | 100% |
B9FFD2 | Oryza sativa subsp. japonica | 41% | 95% |
B9FFD3 | Oryza sativa subsp. japonica | 39% | 100% |
B9FSC8 | Oryza sativa subsp. japonica | 39% | 100% |
C5H429 | Artemisia annua | 39% | 99% |
E9AGH7 | Leishmania infantum | 89% | 100% |
I1RV17 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 32% | 93% |
M1W0Y0 | Claviceps purpurea (strain 20.1) | 32% | 100% |
P0DI08 | Arabidopsis thaliana | 40% | 100% |
P0DI09 | Arabidopsis thaliana | 40% | 100% |
P0DN73 | Streptococcus pyogenes serotype M5 (strain Manfredo) | 28% | 96% |
P40952 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 32% | 96% |
P41816 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 96% |
P43084 | Candida albicans | 33% | 94% |
P54524 | Bacillus subtilis (strain 168) | 34% | 100% |
P77258 | Escherichia coli (strain K12) | 39% | 100% |
Q02899 | Saccharomyces pastorianus | 34% | 96% |
Q03558 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 96% |
Q09670 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
Q09671 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 98% |
Q0E0C6 | Oryza sativa subsp. japonica | 38% | 95% |
Q4QGH6 | Leishmania major | 87% | 100% |
Q4WZ70 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 36% | 100% |
Q5KXG9 | Geobacillus kaustophilus (strain HTA426) | 32% | 100% |
Q69TH4 | Oryza sativa subsp. japonica | 40% | 100% |
Q69TH6 | Oryza sativa subsp. japonica | 41% | 100% |
Q69TH8 | Oryza sativa subsp. japonica | 38% | 100% |
Q69TI0 | Oryza sativa subsp. japonica | 41% | 100% |
Q69TI2 | Oryza sativa subsp. japonica | 39% | 98% |
Q6Z965 | Oryza sativa subsp. japonica | 41% | 97% |
Q6ZXC1 | Claviceps purpurea | 33% | 100% |
Q84QK0 | Oryza sativa subsp. japonica | 40% | 100% |
Q8GYA3 | Arabidopsis thaliana | 37% | 100% |
Q8GYB8 | Arabidopsis thaliana | 38% | 100% |
Q8LAH7 | Arabidopsis thaliana | 39% | 100% |
Q9FEW9 | Solanum lycopersicum | 39% | 97% |
Q9FEX0 | Solanum lycopersicum | 34% | 100% |
Q9FUP0 | Arabidopsis thaliana | 40% | 98% |
Q9XG54 | Solanum lycopersicum | 39% | 100% |
V5BT91 | Trypanosoma cruzi | 46% | 100% |
W6Q2D7 | Penicillium roqueforti (strain FM164) | 39% | 100% |
W6Q9S9 | Penicillium roqueforti (strain FM164) | 38% | 100% |