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 |
Related structures:
AlphaFold database: A4HEY4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 1 |
GO:0051213 | dioxygenase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.722 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.283 |
CLV_PCSK_PC7_1 | 466 | 472 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.321 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.436 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.344 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.410 |
DEG_SPOP_SBC_1 | 475 | 479 | PF00917 | 0.258 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.744 |
DEG_SPOP_SBC_1 | 553 | 557 | PF00917 | 0.223 |
DOC_CYCLIN_yCln2_LP_2 | 292 | 298 | PF00134 | 0.242 |
DOC_CYCLIN_yCln2_LP_2 | 386 | 389 | PF00134 | 0.344 |
DOC_MAPK_DCC_7 | 30 | 39 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 198 | 206 | PF00069 | 0.353 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.223 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 198 | 206 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.223 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.223 |
DOC_PP2B_LxvP_1 | 386 | 389 | PF13499 | 0.338 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.328 |
DOC_PP2B_PxIxI_1 | 34 | 40 | PF00149 | 0.406 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 357 | 360 | PF00568 | 0.382 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.344 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.746 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.451 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 217 | 221 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 274 | 284 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.758 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BIR_III_4 | 454 | 458 | PF00653 | 0.449 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.449 |
LIG_deltaCOP1_diTrp_1 | 422 | 428 | PF00928 | 0.475 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.354 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.313 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.423 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.223 |
LIG_FHA_1 | 307 | 313 | PF00498 | 0.492 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.430 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.453 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.325 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.544 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.410 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.199 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.475 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.658 |
LIG_FXI_DFP_1 | 441 | 445 | PF00024 | 0.449 |
LIG_Integrin_isoDGR_2 | 209 | 211 | PF01839 | 0.328 |
LIG_LIR_Apic_2 | 513 | 517 | PF02991 | 0.223 |
LIG_LIR_Apic_2 | 572 | 578 | PF02991 | 0.343 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 324 | 333 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 372 | 381 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 383 | 389 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.232 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 585 | 589 | PF02991 | 0.465 |
LIG_NRBOX | 279 | 285 | PF00104 | 0.344 |
LIG_NRBOX | 62 | 68 | PF00104 | 0.590 |
LIG_PDZ_Class_2 | 585 | 590 | PF00595 | 0.489 |
LIG_Pex14_1 | 390 | 394 | PF04695 | 0.344 |
LIG_Pex14_1 | 424 | 428 | PF04695 | 0.449 |
LIG_Pex14_2 | 110 | 114 | PF04695 | 0.344 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.332 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.449 |
LIG_SH2_CRK | 375 | 379 | PF00017 | 0.328 |
LIG_SH2_NCK_1 | 220 | 224 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 514 | 517 | PF00017 | 0.363 |
LIG_SH2_SRC | 514 | 517 | PF00017 | 0.363 |
LIG_SH2_SRC | 522 | 525 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 220 | 224 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.333 |
LIG_SH2_STAT3 | 51 | 54 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.311 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.449 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.300 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.288 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.369 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.317 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.475 |
LIG_SH3_3 | 556 | 562 | PF00018 | 0.361 |
LIG_SUMO_SIM_par_1 | 14 | 20 | PF11976 | 0.652 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 579 | 585 | PF11976 | 0.454 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.510 |
LIG_TRAF2_1 | 499 | 502 | PF00917 | 0.475 |
LIG_TRFH_1 | 384 | 388 | PF08558 | 0.344 |
LIG_TYR_ITIM | 312 | 317 | PF00017 | 0.407 |
LIG_UBA3_1 | 404 | 409 | PF00899 | 0.223 |
LIG_WW_2 | 559 | 562 | PF00397 | 0.385 |
MOD_CDK_SPxxK_3 | 204 | 211 | PF00069 | 0.328 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.326 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.322 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.733 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.411 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.277 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.560 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.411 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.465 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.370 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.702 |
MOD_Cter_Amidation | 153 | 156 | PF01082 | 0.223 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.703 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.521 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.420 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.797 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.368 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.490 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.543 |
MOD_N-GLC_2 | 319 | 321 | PF02516 | 0.328 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.748 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.475 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.509 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.409 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.383 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.295 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.356 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.549 |
MOD_NEK2_2 | 517 | 522 | PF00069 | 0.449 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.223 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.223 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.662 |
MOD_PK_1 | 198 | 204 | PF00069 | 0.311 |
MOD_PKA_1 | 471 | 477 | PF00069 | 0.294 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.434 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.363 |
MOD_PKA_2 | 471 | 477 | PF00069 | 0.475 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.702 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.459 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.371 |
MOD_Plk_1 | 571 | 577 | PF00069 | 0.333 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.626 |
MOD_Plk_2-3 | 299 | 305 | PF00069 | 0.449 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.652 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.449 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.449 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.484 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.398 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.408 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.422 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.547 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.328 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.449 |
MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.451 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.437 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.740 |
MOD_SUMO_for_1 | 396 | 399 | PF00179 | 0.329 |
TRG_DiLeu_BaEn_1 | 585 | 590 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.223 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 471 | 473 | PF00400 | 0.223 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9S7 | Leptomonas seymouri | 65% | 100% |
A0A0S4JXF9 | Bodo saltans | 31% | 100% |
A0A1X0NS77 | Trypanosomatidae | 43% | 100% |
A0A3Q8IP66 | Leishmania donovani | 80% | 100% |
A0A3R7K325 | Trypanosoma rangeli | 44% | 100% |
A4I258 | Leishmania infantum | 80% | 100% |
C9ZRU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AYA8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q965 | Leishmania major | 80% | 100% |
V5BED3 | Trypanosoma cruzi | 43% | 100% |