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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQ53
Term | Name | Level | Count |
---|---|---|---|
GO:0006116 | NADH oxidation | 3 | 12 |
GO:0006734 | NADH metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003954 | NADH dehydrogenase activity | 4 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.188 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.263 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 178 | 180 | PF00082 | 0.266 |
CLV_PCSK_PC7_1 | 154 | 160 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.217 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.327 |
DEG_APCC_DBOX_1 | 413 | 421 | PF00400 | 0.320 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.531 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.266 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.251 |
DOC_CKS1_1 | 520 | 525 | PF01111 | 0.473 |
DOC_MAPK_gen_1 | 178 | 186 | PF00069 | 0.251 |
DOC_MAPK_gen_1 | 237 | 244 | PF00069 | 0.295 |
DOC_MAPK_gen_1 | 252 | 259 | PF00069 | 0.182 |
DOC_MAPK_gen_1 | 414 | 421 | PF00069 | 0.314 |
DOC_MAPK_gen_1 | 96 | 105 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.255 |
DOC_MAPK_MEF2A_6 | 414 | 421 | PF00069 | 0.314 |
DOC_MAPK_MEF2A_6 | 8 | 16 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 96 | 105 | PF00069 | 0.285 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.251 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 339 | 343 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.429 |
DOC_USP7_UBL2_3 | 359 | 363 | PF12436 | 0.386 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.251 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 252 | 259 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 443 | 450 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.345 |
LIG_Actin_WH2_2 | 72 | 87 | PF00022 | 0.200 |
LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.335 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.285 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.251 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.248 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.310 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.375 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.466 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.124 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.278 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.251 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.251 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.241 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.256 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.277 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.485 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.658 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.732 |
LIG_LIR_Apic_2 | 134 | 138 | PF02991 | 0.251 |
LIG_LIR_Gen_1 | 118 | 127 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 404 | 413 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 415 | 424 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 442 | 453 | PF02991 | 0.473 |
LIG_LIR_LC3C_4 | 274 | 278 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.251 |
LIG_PDZ_Class_3 | 522 | 527 | PF00595 | 0.479 |
LIG_Pex14_1 | 21 | 25 | PF04695 | 0.251 |
LIG_Pex14_1 | 402 | 406 | PF04695 | 0.293 |
LIG_REV1ctd_RIR_1 | 143 | 152 | PF16727 | 0.266 |
LIG_REV1ctd_RIR_1 | 200 | 208 | PF16727 | 0.310 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.251 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.327 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.391 |
LIG_SH2_CRK | 445 | 449 | PF00017 | 0.520 |
LIG_SH2_PTP2 | 418 | 421 | PF00017 | 0.318 |
LIG_SH2_SRC | 418 | 421 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.251 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 445 | 449 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 475 | 479 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.669 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.251 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.684 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.251 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 380 | 387 | PF11976 | 0.360 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.224 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.400 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.722 |
LIG_TYR_ITIM | 119 | 124 | PF00017 | 0.251 |
LIG_UBA3_1 | 409 | 416 | PF00899 | 0.466 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.266 |
LIG_WRC_WIRS_1 | 229 | 234 | PF05994 | 0.285 |
MOD_CDK_SPxxK_3 | 519 | 526 | PF00069 | 0.739 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.359 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.439 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.299 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.266 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.251 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.245 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.321 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.685 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.310 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.377 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.345 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.307 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.301 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.480 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.556 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.537 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.319 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.280 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.440 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.380 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.345 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.442 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.491 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.583 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.586 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.561 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.254 |
MOD_N-GLC_1 | 210 | 215 | PF02516 | 0.363 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.170 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.309 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.585 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.345 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.450 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.619 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.369 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.469 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.539 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.332 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.308 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.358 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.363 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.280 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.345 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.370 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.594 |
MOD_Plk_1 | 494 | 500 | PF00069 | 0.489 |
MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.310 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.310 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.443 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.310 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.194 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.337 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.251 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.675 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.663 |
MOD_SUMO_rev_2 | 173 | 180 | PF00179 | 0.266 |
MOD_SUMO_rev_2 | 201 | 210 | PF00179 | 0.345 |
MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.345 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.251 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.444 |
TRG_DiLeu_BaEn_3 | 141 | 147 | PF01217 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.251 |
TRG_DiLeu_LyEn_5 | 176 | 181 | PF01217 | 0.251 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.518 |
TRG_ER_diArg_1 | 156 | 159 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.301 |
TRG_NLS_MonoExtN_4 | 154 | 161 | PF00514 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 309 | 313 | PF00026 | 0.394 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P920 | Leptomonas seymouri | 78% | 99% |
A0A0S4IWQ4 | Bodo saltans | 59% | 100% |
A0A1X0P0A4 | Trypanosomatidae | 61% | 100% |
A0A3Q8IL33 | Leishmania donovani | 85% | 100% |
A0A3R7KGC5 | Trypanosoma rangeli | 59% | 100% |
A4IDV2 | Leishmania infantum | 85% | 100% |
D0A465 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9ATX3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
F2Z699 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 32% | 91% |
M0ZYF3 | Solanum tuberosum | 42% | 100% |
O05267 | Bacillus subtilis (strain 168) | 29% | 100% |
O14121 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 96% |
O43090 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 96% |
O80874 | Arabidopsis thaliana | 42% | 100% |
P00393 | Escherichia coli (strain K12) | 27% | 100% |
P32340 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
P40215 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 94% |
P73735 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 25% | 100% |
P80861 | Bacillus subtilis (strain 168) | 23% | 100% |
P95160 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 28% | 100% |
P95200 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q07500 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 97% |
Q2FID4 | Staphylococcus aureus (strain USA300) | 28% | 100% |
Q2FZV7 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 28% | 100% |
Q2YWP9 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 28% | 100% |
Q49W80 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 26% | 100% |
Q4L4V6 | Staphylococcus haemolyticus (strain JCSC1435) | 27% | 100% |
Q4Q0M3 | Leishmania major | 85% | 100% |
Q55CD9 | Dictyostelium discoideum | 39% | 100% |
Q5HHE4 | Staphylococcus aureus (strain COL) | 28% | 100% |
Q5HQM1 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 27% | 100% |
Q6GAY5 | Staphylococcus aureus (strain MSSA476) | 28% | 100% |
Q6GIE7 | Staphylococcus aureus (strain MRSA252) | 28% | 100% |
Q7A6J4 | Staphylococcus aureus (strain N315) | 28% | 100% |
Q8CPV5 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 28% | 100% |
Q8GWA1 | Arabidopsis thaliana | 41% | 100% |
Q8GXR9 | Arabidopsis thaliana | 24% | 100% |
Q8NXG0 | Staphylococcus aureus (strain MW2) | 28% | 100% |
Q99VE0 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 28% | 100% |
Q9SKT7 | Arabidopsis thaliana | 37% | 91% |
Q9ST63 | Solanum tuberosum | 42% | 100% |
V5DLP7 | Trypanosoma cruzi | 60% | 100% |