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: 3 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 15 |
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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HC93
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 3 |
GO:0016874 | ligase activity | 2 | 3 |
GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 3 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.604 |
CLV_MEL_PAP_1 | 264 | 270 | PF00089 | 0.394 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.566 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.548 |
CLV_Separin_Metazoa | 211 | 215 | PF03568 | 0.610 |
DEG_COP1_1 | 409 | 418 | PF00400 | 0.381 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.520 |
DEG_ODPH_VHL_1 | 171 | 183 | PF01847 | 0.450 |
DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.487 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.492 |
DOC_MAPK_gen_1 | 322 | 329 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 403 | 413 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 322 | 329 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 406 | 415 | PF00069 | 0.368 |
DOC_MAPK_RevD_3 | 200 | 216 | PF00069 | 0.641 |
DOC_PP1_RVXF_1 | 356 | 362 | PF00149 | 0.589 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.580 |
DOC_PP2B_PxIxI_1 | 324 | 330 | PF00149 | 0.450 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.684 |
DOC_USP7_UBL2_3 | 219 | 223 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.743 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 39 | 43 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 58 | 64 | PF00244 | 0.443 |
LIG_Actin_WH2_2 | 43 | 60 | PF00022 | 0.527 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.568 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.567 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.502 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.755 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.426 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.486 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.576 |
LIG_KLC1_Yacidic_2 | 281 | 286 | PF13176 | 0.567 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 201 | 207 | PF02991 | 0.737 |
LIG_LIR_Gen_1 | 262 | 271 | PF02991 | 0.478 |
LIG_LIR_LC3C_4 | 313 | 318 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.533 |
LIG_SH2_NCK_1 | 110 | 114 | PF00017 | 0.619 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.710 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 365 | 369 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.710 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.551 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.490 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.569 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.363 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.545 |
LIG_SUMO_SIM_anti_2 | 73 | 81 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.485 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.618 |
LIG_TRAF2_1 | 306 | 309 | PF00917 | 0.597 |
LIG_WRC_WIRS_1 | 50 | 55 | PF05994 | 0.331 |
MOD_CAAXbox | 421 | 424 | PF01239 | 0.570 |
MOD_CDK_SPxxK_3 | 60 | 67 | PF00069 | 0.576 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.543 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.629 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.630 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.622 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.660 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.560 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.567 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.618 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.767 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.337 |
MOD_GlcNHglycan | 31 | 35 | PF01048 | 0.557 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.525 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.491 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.646 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.611 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.413 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.746 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.771 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.496 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.582 |
MOD_N-GLC_1 | 339 | 344 | PF02516 | 0.347 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.597 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.543 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.539 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.525 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.540 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.631 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.612 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.461 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.599 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.288 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.670 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.578 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.592 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.767 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.534 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.353 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.511 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.746 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.573 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.687 |
TRG_DiLeu_BaEn_1 | 74 | 79 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_2 | 64 | 70 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.450 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.606 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P301 | Leptomonas seymouri | 66% | 100% |
A0A0S4IJF4 | Bodo saltans | 38% | 100% |
A0A1X0NUW2 | Trypanosomatidae | 45% | 100% |
A0A3R7KNR3 | Trypanosoma rangeli | 45% | 100% |
A0A3S7WX09 | Leishmania donovani | 77% | 100% |
A4HZS5 | Leishmania infantum | 77% | 100% |
C9ZRK5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AVN0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QBU9 | Leishmania major | 78% | 100% |
V5B5W2 | Trypanosoma cruzi | 34% | 100% |