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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4HCA9
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 2 |
GO:0000963 | mitochondrial RNA processing | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010467 | gene expression | 4 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:0140053 | mitochondrial gene expression | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003729 | mRNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.545 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.538 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 96 | 104 | PF00400 | 0.407 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.450 |
DEG_SPOP_SBC_1 | 204 | 208 | PF00917 | 0.588 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.393 |
DOC_CYCLIN_RxL_1 | 257 | 264 | PF00134 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 262 | 268 | PF00134 | 0.390 |
DOC_MAPK_gen_1 | 329 | 339 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 330 | 339 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 59 | 67 | PF00069 | 0.577 |
DOC_PP1_RVXF_1 | 18 | 24 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.420 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.606 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.543 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.459 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.673 |
LIG_14-3-3_CanoR_1 | 20 | 24 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 203 | 213 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 321 | 325 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 46 | 51 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.577 |
LIG_BIR_III_4 | 225 | 229 | PF00653 | 0.551 |
LIG_deltaCOP1_diTrp_1 | 351 | 359 | PF00928 | 0.500 |
LIG_deltaCOP1_diTrp_1 | 77 | 83 | PF00928 | 0.448 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.617 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.529 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.531 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.663 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.502 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.368 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.543 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.609 |
LIG_LIR_Gen_1 | 232 | 242 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 351 | 359 | PF02991 | 0.382 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 351 | 355 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.496 |
LIG_NRBOX | 257 | 263 | PF00104 | 0.287 |
LIG_SH2_CRK | 234 | 238 | PF00017 | 0.392 |
LIG_SH2_CRK | 386 | 390 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 386 | 390 | PF00017 | 0.426 |
LIG_SH2_SRC | 76 | 79 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 76 | 80 | PF00017 | 0.547 |
LIG_SH2_STAT3 | 278 | 281 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.577 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.452 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.452 |
LIG_SH3_3 | 399 | 405 | PF00018 | 0.547 |
LIG_SUMO_SIM_anti_2 | 333 | 339 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 272 | 279 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 390 | 398 | PF11976 | 0.582 |
LIG_TYR_ITIM | 74 | 79 | PF00017 | 0.556 |
LIG_TYR_ITSM | 230 | 237 | PF00017 | 0.369 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.724 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.494 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.404 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.588 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.572 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.454 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.526 |
MOD_CMANNOS | 80 | 83 | PF00535 | 0.392 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.648 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.551 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.585 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.594 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.586 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.594 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.628 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.423 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.429 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.594 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.495 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.406 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.395 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.652 |
MOD_LATS_1 | 125 | 131 | PF00433 | 0.426 |
MOD_N-GLC_1 | 204 | 209 | PF02516 | 0.439 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.541 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.501 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.435 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.528 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.383 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.717 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.508 |
MOD_NEK2_2 | 273 | 278 | PF00069 | 0.305 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.604 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.737 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.391 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.724 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.580 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.505 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.485 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.595 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.453 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.522 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.420 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.437 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.451 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.451 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.676 |
MOD_SUMO_for_1 | 343 | 346 | PF00179 | 0.383 |
MOD_SUMO_for_1 | 74 | 77 | PF00179 | 0.581 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.531 |
TRG_DiLeu_BaEn_4 | 77 | 83 | PF01217 | 0.380 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.577 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.405 |
TRG_NES_CRM1_1 | 333 | 346 | PF08389 | 0.514 |
TRG_NES_CRM1_1 | 95 | 108 | PF08389 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK37 | Leptomonas seymouri | 71% | 81% |
A0A0N1IKX3 | Leptomonas seymouri | 26% | 75% |
A0A0S4IN88 | Bodo saltans | 43% | 76% |
A0A0S4JQR1 | Bodo saltans | 28% | 76% |
A0A1X0NRA1 | Trypanosomatidae | 27% | 80% |
A0A1X0NTQ0 | Trypanosomatidae | 54% | 85% |
A0A3Q8II17 | Leishmania donovani | 27% | 81% |
A0A3S7WX47 | Leishmania donovani | 88% | 81% |
A0A422NDT8 | Trypanosoma rangeli | 55% | 87% |
A0A422NKD3 | Trypanosoma rangeli | 27% | 84% |
A4HLY4 | Leishmania braziliensis | 27% | 81% |
A4HZU2 | Leishmania infantum | 88% | 81% |
A4I9B3 | Leishmania infantum | 27% | 81% |
C9ZJB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 83% |
C9ZRN1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 86% |
E9AVP7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 81% |
E9B4B3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 81% |
Q4Q3R2 | Leishmania major | 25% | 100% |
Q4QBT2 | Leishmania major | 87% | 100% |
V5BAI0 | Trypanosoma cruzi | 26% | 84% |
V5BVS4 | Trypanosoma cruzi | 55% | 86% |