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: Q4Q7P5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004128 | cytochrome-b5 reductase activity, acting on NAD(P)H | 5 | 2 |
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:0016651 | oxidoreductase activity, acting on NAD(P)H | 3 | 2 |
GO:0016653 | oxidoreductase activity, acting on NAD(P)H, heme protein as acceptor | 4 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.292 |
CLV_C14_Caspase3-7 | 513 | 517 | PF00656 | 0.326 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.160 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.543 |
DEG_SPOP_SBC_1 | 160 | 164 | PF00917 | 0.504 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.259 |
DOC_CKS1_1 | 332 | 337 | PF01111 | 0.292 |
DOC_CKS1_1 | 429 | 434 | PF01111 | 0.394 |
DOC_MAPK_gen_1 | 211 | 220 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 456 | 465 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.601 |
DOC_PP2B_LxvP_1 | 71 | 74 | PF13499 | 0.637 |
DOC_PP4_FxxP_1 | 305 | 308 | PF00568 | 0.326 |
DOC_PP4_FxxP_1 | 332 | 335 | PF00568 | 0.292 |
DOC_PP4_FxxP_1 | 370 | 373 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.666 |
DOC_USP7_MATH_2 | 159 | 165 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 242 | 246 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 428 | 433 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.292 |
LIG_14-3-3_CanoR_1 | 301 | 306 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 447 | 454 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 489 | 495 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 80 | 85 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 249 | 266 | PF00022 | 0.424 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.422 |
LIG_BRCT_BRCA1_1 | 476 | 480 | PF00533 | 0.270 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.330 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.616 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.306 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.418 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.379 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.358 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.586 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.454 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.335 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.292 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.624 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.530 |
LIG_Integrin_isoDGR_2 | 225 | 227 | PF01839 | 0.447 |
LIG_Integrin_isoDGR_2 | 352 | 354 | PF01839 | 0.292 |
LIG_LIR_Apic_2 | 304 | 308 | PF02991 | 0.330 |
LIG_LIR_Apic_2 | 329 | 335 | PF02991 | 0.384 |
LIG_LIR_Apic_2 | 367 | 373 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 231 | 241 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 231 | 236 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 299 | 305 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 417 | 423 | PF02991 | 0.401 |
LIG_OCRL_FandH_1 | 232 | 244 | PF00620 | 0.405 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.335 |
LIG_SH2_CRK | 312 | 316 | PF00017 | 0.270 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.308 |
LIG_SH2_GRB2like | 322 | 325 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 448 | 452 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.349 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.516 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.504 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.271 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.394 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.767 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.292 |
LIG_SUMO_SIM_anti_2 | 100 | 106 | PF11976 | 0.317 |
LIG_SUMO_SIM_anti_2 | 421 | 428 | PF11976 | 0.237 |
LIG_SUMO_SIM_par_1 | 100 | 106 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 196 | 203 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 285 | 293 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 460 | 466 | PF11976 | 0.439 |
LIG_TRAF2_1 | 14 | 17 | PF00917 | 0.788 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.716 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.500 |
LIG_TRFH_1 | 248 | 252 | PF08558 | 0.413 |
LIG_UBA3_1 | 359 | 363 | PF00899 | 0.204 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.349 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.335 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.371 |
MOD_CDC14_SPxK_1 | 261 | 264 | PF00782 | 0.531 |
MOD_CDK_SPxK_1 | 258 | 264 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 331 | 337 | PF00069 | 0.384 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.475 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.287 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.344 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.491 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.430 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.322 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.349 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.319 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.619 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.500 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.696 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.441 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.335 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.573 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.335 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.743 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.359 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.552 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.755 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.560 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.271 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.480 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.314 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.332 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.673 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.436 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.363 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.756 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.465 |
MOD_LATS_1 | 318 | 324 | PF00433 | 0.384 |
MOD_LATS_1 | 5 | 11 | PF00433 | 0.598 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.441 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.384 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.327 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.402 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.287 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.584 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.371 |
MOD_NEK2_2 | 136 | 141 | PF00069 | 0.335 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.335 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.451 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.433 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.405 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.406 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.756 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.272 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.280 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.687 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.255 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.377 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.372 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.300 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.444 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.495 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.464 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.298 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.732 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.527 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.485 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.316 |
MOD_ProDKin_1 | 428 | 434 | PF00069 | 0.394 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.799 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.292 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.150 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.289 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.270 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZN6 | Leptomonas seymouri | 42% | 85% |
A0A1X0P389 | Trypanosomatidae | 34% | 100% |
A0A3Q8IJ69 | Leishmania donovani | 89% | 100% |
A0A422NIH2 | Trypanosoma rangeli | 32% | 100% |
A4HI12 | Leishmania braziliensis | 70% | 100% |
A4I589 | Leishmania infantum | 89% | 100% |
C9ZQM0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B0I6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
V5B7R2 | Trypanosoma cruzi | 35% | 100% |