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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
Related structures:
AlphaFold database: A0A3Q8IN46
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0016491 | oxidoreductase activity | 2 | 16 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 16 |
GO:0017150 | tRNA dihydrouridine synthase activity | 5 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0106413 | dihydrouridine synthase activity | 4 | 16 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 16 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 79 | 83 | PF00656 | 0.675 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.660 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.265 |
DEG_APCC_DBOX_1 | 468 | 476 | PF00400 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 301 | 307 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.459 |
DOC_MAPK_gen_1 | 295 | 305 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.448 |
DOC_PP1_RVXF_1 | 256 | 263 | PF00149 | 0.460 |
DOC_PP2B_LxvP_1 | 301 | 304 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 397 | 400 | PF13499 | 0.628 |
DOC_PP2B_LxvP_1 | 440 | 443 | PF13499 | 0.513 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.516 |
DOC_USP7_MATH_2 | 424 | 430 | PF00917 | 0.354 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 121 | 129 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 411 | 415 | PF00244 | 0.619 |
LIG_14-3-3_CanoR_1 | 469 | 475 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.477 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.551 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.472 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.670 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.590 |
LIG_deltaCOP1_diTrp_1 | 3 | 12 | PF00928 | 0.652 |
LIG_eIF4E_1 | 93 | 99 | PF01652 | 0.459 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.481 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.440 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.552 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.685 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.479 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.589 |
LIG_LIR_Gen_1 | 123 | 130 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 272 | 281 | PF02991 | 0.551 |
LIG_LIR_LC3C_4 | 150 | 155 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 143 | 147 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.433 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.523 |
LIG_Pex14_2 | 384 | 388 | PF04695 | 0.590 |
LIG_SH2_CRK | 93 | 97 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 412 | 416 | PF00017 | 0.590 |
LIG_SH2_PTP2 | 456 | 459 | PF00017 | 0.426 |
LIG_SH2_SRC | 484 | 487 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 124 | 128 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.652 |
LIG_SH2_STAP1 | 8 | 12 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 343 | 346 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.615 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.492 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.553 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.477 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.638 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 463 | 470 | PF11976 | 0.527 |
LIG_TRAF2_1 | 477 | 480 | PF00917 | 0.428 |
LIG_WW_3 | 364 | 368 | PF00397 | 0.579 |
MOD_CDK_SPK_2 | 420 | 425 | PF00069 | 0.584 |
MOD_CDK_SPxxK_3 | 133 | 140 | PF00069 | 0.551 |
MOD_CDK_SPxxK_3 | 455 | 462 | PF00069 | 0.386 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.430 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.500 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.556 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.763 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.366 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.589 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.540 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.671 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.645 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.604 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.392 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.759 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.245 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.218 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.566 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.254 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.272 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.577 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.665 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.449 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.581 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.483 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.475 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.465 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.463 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.693 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.661 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.619 |
MOD_LATS_1 | 277 | 283 | PF00433 | 0.515 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.393 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.515 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.478 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.495 |
MOD_N-GLC_2 | 229 | 231 | PF02516 | 0.204 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.456 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.462 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.744 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.641 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.379 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.758 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.499 |
MOD_OFUCOSY | 231 | 236 | PF10250 | 0.204 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.441 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.360 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.462 |
MOD_PKA_2 | 410 | 416 | PF00069 | 0.605 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.477 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.691 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.403 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.567 |
MOD_Plk_1 | 470 | 476 | PF00069 | 0.413 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.522 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.551 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.418 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.551 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.699 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.544 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.434 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.551 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.437 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.760 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.614 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.604 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.412 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.541 |
TRG_DiLeu_BaEn_1 | 292 | 297 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 256 | 258 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT7 | Leptomonas seymouri | 69% | 96% |
A0A0S4JTG4 | Bodo saltans | 44% | 100% |
A0A1X0PAA8 | Trypanosomatidae | 45% | 100% |
A0A3Q8IJ00 | Leishmania donovani | 23% | 100% |
A0A3R7KZP3 | Trypanosoma rangeli | 46% | 100% |
A4HAN2 | Leishmania braziliensis | 78% | 100% |
A4HNQ5 | Leishmania braziliensis | 24% | 100% |
A4I9S4 | Leishmania infantum | 99% | 100% |
A4ICU0 | Leishmania infantum | 23% | 100% |
C9ZMV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9ASG4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
E9B4T5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q391 | Leishmania major | 92% | 100% |
V5DJT2 | Trypanosoma cruzi | 46% | 100% |