Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HI12
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 10 |
GO:0008940 | nitrate reductase activity | 4 | 8 |
GO:0009703 | nitrate reductase (NADH) activity | 6 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 11 |
GO:0016661 | oxidoreductase activity, acting on other nitrogenous compounds as donors | 3 | 8 |
GO:0020037 | heme binding | 4 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046857 | oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor | 4 | 8 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046906 | tetrapyrrole binding | 3 | 10 |
GO:0050463 | nitrate reductase [NAD(P)H] activity | 5 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0004128 | cytochrome-b5 reductase activity, acting on NAD(P)H | 5 | 1 |
GO:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 1 |
GO:0016653 | oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 470 | 474 | PF00656 | 0.227 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.591 |
DEG_SCF_FBW7_1 | 406 | 411 | PF00400 | 0.298 |
DEG_SCF_FBW7_1 | 50 | 56 | PF00400 | 0.700 |
DEG_SPOP_SBC_1 | 476 | 480 | PF00917 | 0.344 |
DOC_CKS1_1 | 430 | 435 | PF01111 | 0.441 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.698 |
DOC_MAPK_gen_1 | 195 | 202 | PF00069 | 0.238 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 363 | 371 | PF00069 | 0.305 |
DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.449 |
DOC_MAPK_NFAT4_5 | 195 | 203 | PF00069 | 0.354 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.595 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.753 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.684 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.253 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.794 |
LIG_14-3-3_CanoR_1 | 188 | 193 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 332 | 337 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 468 | 476 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.570 |
LIG_Actin_WH2_2 | 250 | 267 | PF00022 | 0.513 |
LIG_BIR_III_2 | 11 | 15 | PF00653 | 0.552 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.363 |
LIG_CtBP_PxDLS_1 | 66 | 71 | PF00389 | 0.551 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.392 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.722 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.549 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.446 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.547 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.408 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.454 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.354 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.480 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.424 |
LIG_Integrin_isoDGR_2 | 226 | 228 | PF01839 | 0.480 |
LIG_LIR_Apic_2 | 368 | 374 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 459 | 466 | PF02991 | 0.227 |
LIG_LIR_LC3C_4 | 99 | 104 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 459 | 463 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.573 |
LIG_MLH1_MIPbox_1 | 356 | 360 | PF16413 | 0.434 |
LIG_NRBOX | 218 | 224 | PF00104 | 0.349 |
LIG_PDZ_Class_2 | 532 | 537 | PF00595 | 0.348 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.532 |
LIG_Pex14_2 | 371 | 375 | PF04695 | 0.375 |
LIG_REV1ctd_RIR_1 | 358 | 368 | PF16727 | 0.466 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.498 |
LIG_SH2_CRK | 81 | 85 | PF00017 | 0.545 |
LIG_SH2_GRB2like | 323 | 326 | PF00017 | 0.534 |
LIG_SH2_PTP2 | 319 | 322 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.227 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.452 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.306 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.626 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.403 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.441 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.791 |
LIG_SUMO_SIM_anti_2 | 101 | 107 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 461 | 467 | PF11976 | 0.468 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.740 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.789 |
LIG_TRFH_1 | 249 | 253 | PF08558 | 0.480 |
LIG_UBA3_1 | 289 | 293 | PF00899 | 0.307 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.408 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.512 |
LIG_WRC_WIRS_1 | 341 | 346 | PF05994 | 0.465 |
MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.547 |
MOD_CDC14_SPxK_1 | 262 | 265 | PF00782 | 0.685 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.553 |
MOD_CDK_SPxK_1 | 206 | 212 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 259 | 265 | PF00069 | 0.685 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.487 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.472 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.555 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.480 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.431 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.493 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.451 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.354 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.541 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.459 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.480 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.735 |
MOD_GlcNHglycan | 26 | 30 | PF01048 | 0.746 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.611 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.647 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.512 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.542 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.330 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.755 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.810 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.434 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.578 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.611 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.455 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.448 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.327 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.342 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.781 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.480 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.659 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.646 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.508 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.266 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.507 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.488 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.328 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.411 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.482 |
MOD_PIKK_1 | 274 | 280 | PF00454 | 0.548 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.480 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.227 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.494 |
MOD_PK_1 | 188 | 194 | PF00069 | 0.332 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.543 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.506 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.298 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.252 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.480 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.337 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.285 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.227 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.480 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.425 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.482 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.292 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.370 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.589 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.429 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.657 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.253 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.441 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.794 |
MOD_SUMO_for_1 | 337 | 340 | PF00179 | 0.305 |
MOD_SUMO_rev_2 | 286 | 295 | PF00179 | 0.364 |
TRG_DiLeu_BaEn_1 | 89 | 94 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_4 | 440 | 446 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_4 | 67 | 73 | PF01217 | 0.665 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.203 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 188 | 193 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN6 | Leptomonas seymouri | 42% | 85% |
A0A1X0P389 | Trypanosomatidae | 32% | 100% |
A0A3Q8IJ69 | Leishmania donovani | 71% | 100% |
A0A422NIH2 | Trypanosoma rangeli | 32% | 100% |
A4I589 | Leishmania infantum | 71% | 100% |
C9ZQM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B0I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q7P5 | Leishmania major | 70% | 100% |
V5B7R2 | Trypanosoma cruzi | 33% | 100% |