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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S7WR58
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 | 0.357 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.418 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 56 | 62 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.370 |
DEG_APCC_DBOX_1 | 374 | 382 | PF00400 | 0.459 |
DOC_MAPK_FxFP_2 | 122 | 125 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 162 | 172 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.576 |
DOC_MAPK_JIP1_4 | 30 | 36 | PF00069 | 0.509 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.374 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.424 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.298 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.378 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.609 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.395 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.414 |
LIG_Actin_WH2_2 | 14 | 32 | PF00022 | 0.554 |
LIG_eIF4E_1 | 312 | 318 | PF01652 | 0.404 |
LIG_EVH1_2 | 120 | 124 | PF00568 | 0.439 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.617 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.360 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.348 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.531 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.315 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.315 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 193 | 199 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 232 | 241 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 359 | 367 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.685 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.394 |
LIG_MYND_1 | 27 | 31 | PF01753 | 0.615 |
LIG_NRBOX | 341 | 347 | PF00104 | 0.372 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.465 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 296 | 300 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 445 | 449 | PF00017 | 0.588 |
LIG_SH2_PTP2 | 19 | 22 | PF00017 | 0.667 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.348 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.396 |
LIG_SH2_SRC | 272 | 275 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.313 |
LIG_SH2_STAP1 | 65 | 69 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 19 | 22 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.546 |
LIG_SH3_1 | 19 | 25 | PF00018 | 0.569 |
LIG_SH3_2 | 118 | 123 | PF14604 | 0.467 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.573 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.561 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.660 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.618 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 408 | 414 | PF11976 | 0.414 |
LIG_TYR_ITIM | 360 | 365 | PF00017 | 0.412 |
LIG_WW_1 | 16 | 19 | PF00397 | 0.569 |
MOD_CDK_SPK_2 | 344 | 349 | PF00069 | 0.253 |
MOD_CDK_SPxxK_3 | 276 | 283 | PF00069 | 0.313 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.678 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.491 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.320 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.291 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.343 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.487 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.594 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.620 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.368 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.598 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.477 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.677 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.677 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.746 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.561 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.458 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.442 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.362 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.361 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.535 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.551 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.642 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.647 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.382 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.495 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.623 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.405 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.581 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.387 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.496 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.448 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.542 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.462 |
MOD_PIKK_1 | 242 | 248 | PF00454 | 0.381 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.449 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.460 |
MOD_PK_1 | 356 | 362 | PF00069 | 0.434 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.543 |
MOD_Plk_2-3 | 304 | 310 | PF00069 | 0.273 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.402 |
MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.395 |
TRG_DiLeu_BaEn_2 | 398 | 404 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 213 | 218 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.396 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.512 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5I8 | Leptomonas seymouri | 46% | 100% |
A0A0N1I4X2 | Leptomonas seymouri | 70% | 100% |
A0A0N1I9E8 | Leptomonas seymouri | 23% | 100% |
A0A0N1PDX1 | Leptomonas seymouri | 23% | 100% |
A0A0S4ILS9 | Bodo saltans | 28% | 100% |
A0A0S4JMB1 | Bodo saltans | 28% | 100% |
A0A1X0NRR2 | Trypanosomatidae | 46% | 98% |
A0A1X0NZZ5 | Trypanosomatidae | 23% | 100% |
A0A3Q8IRG0 | Leishmania donovani | 27% | 100% |
A0A3S7WR50 | Leishmania donovani | 45% | 98% |
A0A482N9T9 | Talaromyces variabilis | 23% | 100% |
A4H648 | Leishmania braziliensis | 44% | 98% |
A4H649 | Leishmania braziliensis | 85% | 100% |
A4HUG8 | Leishmania infantum | 45% | 98% |
A4HUG9 | Leishmania infantum | 100% | 100% |
A4IE56 | Leishmania infantum | 27% | 100% |
C9ZVI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
D7UPN2 | Alternaria alternata | 27% | 100% |
E9AN66 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 98% |
E9AN67 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9ATK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
K4BW79 | Solanum lycopersicum | 27% | 100% |
P0DO31 | Neonectria sp. (strain DH2) | 23% | 100% |
P42328 | Geobacillus stearothermophilus | 25% | 100% |
P43903 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 25% | 100% |
P47199 | Mus musculus | 26% | 100% |
Q0VC50 | Bos taurus | 25% | 100% |
Q4QHF8 | Leishmania major | 95% | 100% |
Q4QHF9 | Leishmania major | 44% | 96% |
Q4W4Z2 | Caenorhabditis elegans | 26% | 100% |
Q5HM44 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 24% | 100% |
Q5JI69 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 25% | 100% |
Q7T3C7 | Danio rerio | 24% | 100% |
Q8CRJ7 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 24% | 100% |
Q8H0M1 | Spinacia oleracea | 27% | 100% |
Q8JFV8 | Danio rerio | 26% | 99% |
Q8KQL2 | Enterococcus avium | 24% | 100% |
Q8WWV3 | Homo sapiens | 25% | 100% |
Q924D0 | Mus musculus | 25% | 100% |
Q99536 | Homo sapiens | 27% | 100% |
Q9SV68 | Arabidopsis thaliana | 26% | 100% |
Q9ZUC1 | Arabidopsis thaliana | 28% | 100% |
V5ALK9 | Trypanosoma cruzi | 48% | 100% |
V5B1P3 | Trypanosoma cruzi | 27% | 100% |