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: A0A3Q8IJ69
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 | 133 | 137 | PF00656 | 0.402 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.389 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.169 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.562 |
DEG_SCF_FBW7_1 | 50 | 56 | PF00400 | 0.699 |
DEG_SPOP_SBC_1 | 6 | 10 | PF00917 | 0.578 |
DOC_CKS1_1 | 333 | 338 | PF01111 | 0.442 |
DOC_CKS1_1 | 430 | 435 | PF01111 | 0.441 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.699 |
DOC_MAPK_gen_1 | 212 | 221 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.449 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.767 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.389 |
DOC_PP4_FxxP_1 | 333 | 336 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 371 | 374 | PF00568 | 0.474 |
DOC_USP7_UBL2_3 | 243 | 247 | PF12436 | 0.346 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.817 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 294 | 304 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 448 | 455 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 490 | 496 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.779 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.582 |
LIG_APCC_ABBA_1 | 199 | 204 | PF00400 | 0.424 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.266 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.344 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.738 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.323 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.490 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.382 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.404 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.406 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.447 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.480 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.402 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.723 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.400 |
LIG_Integrin_isoDGR_2 | 226 | 228 | PF01839 | 0.480 |
LIG_Integrin_isoDGR_2 | 353 | 355 | PF01839 | 0.402 |
LIG_LIR_Apic_2 | 305 | 309 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 330 | 336 | PF02991 | 0.414 |
LIG_LIR_Apic_2 | 368 | 374 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.391 |
LIG_MLH1_MIPbox_1 | 356 | 360 | PF16413 | 0.383 |
LIG_OCRL_FandH_1 | 233 | 245 | PF00620 | 0.363 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.480 |
LIG_REV1ctd_RIR_1 | 358 | 368 | PF16727 | 0.383 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 323 | 326 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.408 |
LIG_SH3_1 | 260 | 266 | PF00018 | 0.439 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.422 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.589 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.562 |
LIG_SH3_3 | 371 | 377 | PF00018 | 0.335 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.441 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.781 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.448 |
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 | 197 | 204 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 461 | 467 | PF11976 | 0.468 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.816 |
LIG_TRAF2_1 | 167 | 170 | PF00917 | 0.759 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.514 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.786 |
LIG_TRFH_1 | 249 | 253 | PF08558 | 0.480 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.408 |
LIG_WRC_WIRS_1 | 303 | 308 | PF05994 | 0.480 |
MOD_CDC14_SPxK_1 | 262 | 265 | PF00782 | 0.562 |
MOD_CDK_SPxK_1 | 206 | 212 | PF00069 | 0.429 |
MOD_CDK_SPxK_1 | 259 | 265 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 332 | 338 | PF00069 | 0.421 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.487 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.429 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.493 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.479 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.458 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.400 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.493 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.249 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.599 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.787 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.772 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.533 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.755 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.459 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.480 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.680 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.490 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.746 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.375 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.518 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.564 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.725 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.385 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.318 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.419 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.785 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.449 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.430 |
MOD_LATS_1 | 319 | 325 | PF00433 | 0.434 |
MOD_LATS_1 | 5 | 11 | PF00433 | 0.679 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.519 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.342 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.434 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.646 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.335 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.667 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.411 |
MOD_NEK2_2 | 137 | 142 | PF00069 | 0.480 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.493 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.480 |
MOD_PIKK_1 | 529 | 535 | PF00454 | 0.504 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.430 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.448 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.463 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.778 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.337 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.396 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.480 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.471 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.481 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.402 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.335 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.696 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.744 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.383 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.575 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.326 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.441 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.815 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.454 |
TRG_DiLeu_BaEn_1 | 89 | 94 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_4 | 67 | 73 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.150 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.227 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 442 | 444 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 288 | 293 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN6 | Leptomonas seymouri | 44% | 85% |
A0A1X0P389 | Trypanosomatidae | 34% | 100% |
A0A422NIH2 | Trypanosoma rangeli | 33% | 100% |
A4HI12 | Leishmania braziliensis | 71% | 100% |
A4I589 | Leishmania infantum | 99% | 100% |
C9ZQM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B0I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q7P5 | Leishmania major | 89% | 100% |
V5B7R2 | Trypanosoma cruzi | 35% | 100% |