Oxidoreductase, Ferredoxin NADP+ reductase-like
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:0005747 | mitochondrial respiratory chain complex I | 4 | 1 |
GO:0030964 | NADH dehydrogenase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045271 | respiratory chain complex I | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:0098803 | respiratory chain complex | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990204 | oxidoreductase complex | 3 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HZ41
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004324 | ferredoxin-NADP+ reductase activity | 6 | 5 |
GO:0008937 | ferredoxin-NAD(P) reductase activity | 5 | 5 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016730 | oxidoreductase activity, acting on iron-sulfur proteins as donors | 3 | 7 |
GO:0016731 | oxidoreductase activity, acting on iron-sulfur proteins as donors, NAD or NADP as acceptor | 4 | 7 |
GO:0015039 | NADPH-adrenodoxin reductase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.423 |
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.404 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 230 | 234 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 232 | 234 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 232 | 234 | PF00082 | 0.454 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 661 | 665 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 401 | 409 | PF00400 | 0.381 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.541 |
DEG_SCF_FBW7_1 | 649 | 654 | PF00400 | 0.640 |
DEG_SPOP_SBC_1 | 48 | 52 | PF00917 | 0.600 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.747 |
DEG_SPOP_SBC_1 | 574 | 578 | PF00917 | 0.666 |
DOC_ANK_TNKS_1 | 232 | 239 | PF00023 | 0.467 |
DOC_ANK_TNKS_1 | 428 | 435 | PF00023 | 0.583 |
DOC_CYCLIN_RxL_1 | 105 | 116 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 658 | 668 | PF00134 | 0.602 |
DOC_CYCLIN_yCln2_LP_2 | 121 | 127 | PF00134 | 0.343 |
DOC_MAPK_DCC_7 | 400 | 410 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.366 |
DOC_MAPK_gen_1 | 230 | 237 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 330 | 338 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 592 | 599 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 85 | 92 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 627 | 634 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 85 | 92 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 108 | 116 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 152 | 158 | PF00149 | 0.356 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.328 |
DOC_PP2B_LxvP_1 | 191 | 194 | PF13499 | 0.402 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.713 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 268 | 272 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 494 | 498 | PF12436 | 0.262 |
DOC_USP7_UBL2_3 | 618 | 622 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.615 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.338 |
LIG_AP2alpha_1 | 146 | 150 | PF02296 | 0.393 |
LIG_APCC_ABBA_1 | 111 | 116 | PF00400 | 0.423 |
LIG_BIR_III_4 | 359 | 363 | PF00653 | 0.583 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.429 |
LIG_BRCT_BRCA1_1 | 97 | 101 | PF00533 | 0.444 |
LIG_CtBP_PxDLS_1 | 613 | 618 | PF00389 | 0.432 |
LIG_eIF4E_1 | 419 | 425 | PF01652 | 0.511 |
LIG_eIF4E_1 | 580 | 586 | PF01652 | 0.478 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.413 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.483 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.400 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.473 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.764 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.549 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.604 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 143 | 150 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 40 | 48 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 440 | 451 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 206 | 210 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.494 |
LIG_NRBOX | 659 | 665 | PF00104 | 0.482 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.333 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.317 |
LIG_SH2_CRK | 211 | 215 | PF00017 | 0.431 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.485 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.525 |
LIG_SH2_GRB2like | 210 | 213 | PF00017 | 0.324 |
LIG_SH2_SRC | 302 | 305 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.485 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.358 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.532 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.646 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.611 |
LIG_SUMO_SIM_anti_2 | 276 | 282 | PF11976 | 0.476 |
LIG_SUMO_SIM_anti_2 | 406 | 413 | PF11976 | 0.484 |
LIG_SUMO_SIM_anti_2 | 553 | 559 | PF11976 | 0.758 |
LIG_TRAF2_1 | 345 | 348 | PF00917 | 0.555 |
LIG_TRFH_1 | 403 | 407 | PF08558 | 0.381 |
LIG_UBA3_1 | 657 | 661 | PF00899 | 0.626 |
LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.768 |
MOD_CDK_SPK_2 | 217 | 222 | PF00069 | 0.358 |
MOD_CDK_SPxK_1 | 563 | 569 | PF00069 | 0.685 |
MOD_CDK_SPxK_1 | 647 | 653 | PF00069 | 0.625 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.443 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.634 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.531 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.688 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.675 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.702 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.655 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.322 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.455 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.504 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.676 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.650 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.545 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.654 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.626 |
MOD_Cter_Amidation | 616 | 619 | PF01082 | 0.449 |
MOD_Cter_Amidation | 638 | 641 | PF01082 | 0.450 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.380 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.402 |
MOD_GlcNHglycan | 287 | 291 | PF01048 | 0.376 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.613 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.680 |
MOD_GlcNHglycan | 374 | 378 | PF01048 | 0.736 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.716 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.745 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.716 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.663 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.621 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.347 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.341 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.683 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.461 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.536 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.630 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.618 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.671 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.734 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.715 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.601 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.664 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.614 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.405 |
MOD_N-GLC_1 | 403 | 408 | PF02516 | 0.473 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.719 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.701 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.412 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.335 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.565 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.521 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.357 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.638 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.497 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.419 |
MOD_NEK2_2 | 4 | 9 | PF00069 | 0.612 |
MOD_NEK2_2 | 575 | 580 | PF00069 | 0.557 |
MOD_PK_1 | 42 | 48 | PF00069 | 0.535 |
MOD_PK_1 | 458 | 464 | PF00069 | 0.455 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.347 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.440 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.641 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.616 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.695 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.616 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.401 |
MOD_Plk_1 | 286 | 292 | PF00069 | 0.418 |
MOD_Plk_2-3 | 551 | 557 | PF00069 | 0.640 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.353 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.421 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.430 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.351 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.569 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.483 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.431 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.436 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.730 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.436 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.685 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.621 |
MOD_SUMO_for_1 | 307 | 310 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 133 | 142 | PF00179 | 0.360 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.540 |
TRG_NLS_Bipartite_1 | 416 | 430 | PF00514 | 0.474 |
TRG_NLS_MonoExtC_3 | 425 | 431 | PF00514 | 0.529 |
TRG_NLS_MonoExtN_4 | 84 | 89 | PF00514 | 0.576 |
TRG_Pf-PMV_PEXEL_1 | 604 | 609 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 671 | 676 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDQ8 | Leptomonas seymouri | 67% | 99% |
A0A0S4J2F1 | Bodo saltans | 43% | 100% |
A0A1X0NYU3 | Trypanosomatidae | 52% | 100% |
A0A3S5H794 | Leishmania donovani | 100% | 100% |
A0A422MZJ3 | Trypanosoma rangeli | 52% | 100% |
A4HBP0 | Leishmania braziliensis | 85% | 100% |
D0A1P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AV09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P22570 | Homo sapiens | 35% | 100% |
P56522 | Rattus norvegicus | 35% | 100% |
P65529 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P82861 | Salvelinus fontinalis | 31% | 100% |
P9WJI0 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WJI1 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q4QCH3 | Leishmania major | 95% | 100% |
Q54KG7 | Dictyostelium discoideum | 27% | 100% |
Q61578 | Mus musculus | 32% | 100% |
Q8W3L1 | Arabidopsis thaliana | 30% | 100% |
Q9V3T9 | Drosophila melanogaster | 29% | 100% |
V5BQ55 | Trypanosoma cruzi | 55% | 100% |