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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q9N2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051537 | 2 iron, 2 sulfur cluster binding | 4 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 2 |
GO:0008942 | nitrite reductase [NAD(P)H] activity | 5 | 1 |
GO:0016661 | oxidoreductase activity, acting on other nitrogenous compounds as donors | 3 | 1 |
GO:0046857 | oxidoreductase activity, acting on other nitrogenous compounds as donors, with NAD or NADP as acceptor | 4 | 1 |
GO:0098809 | nitrite reductase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.686 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 364 | 366 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.404 |
CLV_PCSK_PC7_1 | 360 | 366 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.401 |
CLV_Separin_Metazoa | 299 | 303 | PF03568 | 0.427 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.343 |
DOC_CDC14_PxL_1 | 413 | 421 | PF14671 | 0.452 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.343 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 110 | 118 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.452 |
DOC_MAPK_gen_1 | 447 | 457 | PF00069 | 0.528 |
DOC_MAPK_JIP1_4 | 150 | 156 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 451 | 459 | PF00069 | 0.469 |
DOC_PP1_RVXF_1 | 12 | 19 | PF00149 | 0.343 |
DOC_PP1_RVXF_1 | 367 | 373 | PF00149 | 0.395 |
DOC_PP2B_LxvP_1 | 163 | 166 | PF13499 | 0.593 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.377 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.525 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.415 |
DOC_USP7_MATH_2 | 211 | 217 | PF00917 | 0.602 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.475 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 198 | 204 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 217 | 224 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 227 | 235 | PF00244 | 0.485 |
LIG_Actin_WH2_2 | 241 | 258 | PF00022 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 313 | 317 | PF00533 | 0.581 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.454 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.343 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.464 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.479 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.551 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.326 |
LIG_LIR_Gen_1 | 122 | 133 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 262 | 270 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 314 | 324 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 380 | 390 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 456 | 465 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 262 | 266 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.372 |
LIG_MYND_3 | 416 | 420 | PF01753 | 0.396 |
LIG_Pex14_1 | 425 | 429 | PF04695 | 0.518 |
LIG_PTB_Apo_2 | 389 | 396 | PF02174 | 0.362 |
LIG_PTB_Apo_2 | 44 | 51 | PF02174 | 0.263 |
LIG_PTB_Phospho_1 | 389 | 395 | PF10480 | 0.353 |
LIG_PTB_Phospho_1 | 44 | 50 | PF10480 | 0.262 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.349 |
LIG_SH2_PTP2 | 125 | 128 | PF00017 | 0.395 |
LIG_SH2_PTP2 | 263 | 266 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.530 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.360 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.355 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 54 | 60 | PF11976 | 0.343 |
LIG_UBA3_1 | 316 | 322 | PF00899 | 0.361 |
MOD_CDK_SPK_2 | 96 | 101 | PF00069 | 0.396 |
MOD_CDK_SPxxK_3 | 220 | 227 | PF00069 | 0.545 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.420 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.661 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.788 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.600 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.693 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.603 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.634 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.731 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.720 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.587 |
MOD_Cter_Amidation | 12 | 15 | PF01082 | 0.415 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.693 |
MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.478 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.531 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.663 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.439 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.575 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.509 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.547 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.532 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.644 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.408 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.435 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.527 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.528 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.649 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.499 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.415 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.529 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.488 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.532 |
MOD_N-GLC_1 | 495 | 500 | PF02516 | 0.397 |
MOD_N-GLC_2 | 47 | 49 | PF02516 | 0.271 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.590 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.333 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.411 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.582 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.382 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.319 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.479 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.466 |
MOD_PKA_1 | 303 | 309 | PF00069 | 0.372 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.704 |
MOD_PKA_2 | 272 | 278 | PF00069 | 0.448 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.372 |
MOD_PKA_2 | 359 | 365 | PF00069 | 0.448 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.452 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.406 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.584 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.506 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.450 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.443 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.616 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.485 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.747 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.420 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.724 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.478 |
MOD_SUMO_for_1 | 417 | 420 | PF00179 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.535 |
TRG_DiLeu_BaLyEn_6 | 52 | 57 | PF01217 | 0.271 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 301 | 304 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 489 | 492 | PF00400 | 0.447 |
TRG_NES_CRM1_1 | 259 | 272 | PF08389 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8I7 | Leptomonas seymouri | 58% | 100% |
A0A0S4JP70 | Bodo saltans | 38% | 100% |
A0A1X0NYR2 | Trypanosomatidae | 37% | 100% |
A0A3S5ISQ1 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WZH8 | Leishmania donovani | 92% | 100% |
A4HEA9 | Leishmania braziliensis | 72% | 99% |
A4I1Q5 | Leishmania infantum | 91% | 100% |
C9ZKA9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AXT9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BS23 | Trypanosoma cruzi | 35% | 100% |