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: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005794 | Golgi apparatus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4QHF8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 16 |
GO:0016491 | oxidoreductase activity | 2 | 16 |
GO:0003960 | NADPH:quinone reductase activity | 5 | 1 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 1 |
GO:0016655 | oxidoreductase activity, acting on NAD(P)H, quinone or similar compound as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 307 | 311 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.381 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.483 |
CLV_PCSK_PC7_1 | 56 | 62 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.340 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.418 |
DOC_MAPK_FxFP_2 | 122 | 125 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 162 | 172 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.578 |
DOC_MAPK_JIP1_4 | 30 | 36 | PF00069 | 0.523 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.342 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.416 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.392 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.261 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.517 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.227 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.368 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.540 |
LIG_eIF4E_1 | 312 | 318 | PF01652 | 0.370 |
LIG_EVH1_2 | 120 | 124 | PF00568 | 0.410 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.568 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.328 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.224 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.335 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.538 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.277 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.147 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.404 |
LIG_LIR_Apic_2 | 193 | 199 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 359 | 367 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.353 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.624 |
LIG_NRBOX | 341 | 347 | PF00104 | 0.334 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.584 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.307 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.355 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.498 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.548 |
LIG_SH3_2 | 118 | 123 | PF14604 | 0.447 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.749 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.549 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.546 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.591 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.417 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.654 |
LIG_SUMO_SIM_anti_2 | 408 | 415 | PF11976 | 0.392 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.379 |
LIG_TYR_ITIM | 360 | 365 | PF00017 | 0.371 |
LIG_WW_1 | 16 | 19 | PF00397 | 0.552 |
MOD_CDK_SPK_2 | 344 | 349 | PF00069 | 0.227 |
MOD_CDK_SPxxK_3 | 276 | 283 | PF00069 | 0.273 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.723 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.475 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.275 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.254 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.376 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.512 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.636 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.621 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.337 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.590 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.495 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.656 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.639 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.506 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.525 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.448 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.418 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.332 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.321 |
MOD_GlcNHglycan | 35 | 39 | PF01048 | 0.591 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.473 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.599 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.655 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.677 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.398 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.522 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.626 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.554 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.359 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.423 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.569 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.405 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.567 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.340 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.436 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.436 |
MOD_PK_1 | 356 | 362 | PF00069 | 0.392 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.587 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.624 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.519 |
MOD_Plk_2-3 | 304 | 310 | PF00069 | 0.242 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.368 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.360 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.520 |
TRG_DiLeu_BaEn_2 | 398 | 404 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3I0 | Leptomonas seymouri | 23% | 100% |
A0A0N0P5I8 | Leptomonas seymouri | 45% | 100% |
A0A0N1I4X2 | Leptomonas seymouri | 70% | 100% |
A0A0N1I9E8 | Leptomonas seymouri | 24% | 100% |
A0A0N1PDX1 | Leptomonas seymouri | 24% | 100% |
A0A0S4ILS9 | Bodo saltans | 27% | 100% |
A0A0S4JMB1 | Bodo saltans | 28% | 100% |
A0A1X0NRR2 | Trypanosomatidae | 49% | 98% |
A0A1X0NZZ5 | Trypanosomatidae | 23% | 100% |
A0A3Q8ICJ5 | Leishmania donovani | 24% | 100% |
A0A3Q8IRG0 | Leishmania donovani | 28% | 100% |
A0A3S7WR50 | Leishmania donovani | 43% | 100% |
A0A3S7WR58 | Leishmania donovani | 95% | 100% |
A4H648 | Leishmania braziliensis | 44% | 100% |
A4H649 | Leishmania braziliensis | 84% | 100% |
A4HUG8 | Leishmania infantum | 43% | 100% |
A4HUG9 | Leishmania infantum | 95% | 100% |
A4I0D8 | Leishmania infantum | 24% | 100% |
A4IE56 | Leishmania infantum | 28% | 100% |
C9ZVI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
D7UPN2 | Alternaria alternata | 27% | 100% |
E9AN66 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9ATK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9AWA2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
K4BW79 | Solanum lycopersicum | 27% | 100% |
P12311 | Geobacillus stearothermophilus | 25% | 100% |
Q0VC50 | Bos taurus | 25% | 100% |
Q4Q0Z7 | Leishmania major | 27% | 100% |
Q4QB77 | Leishmania major | 24% | 100% |
Q4QHF9 | Leishmania major | 42% | 100% |
Q4W4Z2 | Caenorhabditis elegans | 26% | 100% |
Q7T3C7 | Danio rerio | 23% | 100% |
Q8BGC4 | Mus musculus | 23% | 100% |
Q8H0M1 | Spinacia oleracea | 26% | 100% |
Q8JFV8 | Danio rerio | 26% | 99% |
Q8KQL2 | Enterococcus avium | 23% | 100% |
Q8WWV3 | Homo sapiens | 25% | 100% |
Q924D0 | Mus musculus | 26% | 100% |
Q99536 | Homo sapiens | 26% | 100% |
Q9AYU1 | Triphysaria versicolor | 24% | 100% |
Q9P4C2 | Kluyveromyces marxianus | 26% | 100% |
Q9SV68 | Arabidopsis thaliana | 25% | 100% |
Q9ZUC1 | Arabidopsis thaliana | 28% | 100% |
V5ALK9 | Trypanosoma cruzi | 46% | 100% |
V5B1P3 | Trypanosoma cruzi | 28% | 100% |