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:0005737 | cytoplasm | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AFF9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006364 | rRNA processing | 8 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0016072 | rRNA metabolic process | 7 | 12 |
GO:0032259 | methylation | 2 | 12 |
GO:0034470 | ncRNA processing | 7 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034660 | ncRNA metabolic process | 6 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0008168 | methyltransferase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 424 | 426 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.572 |
CLV_PCSK_FUR_1 | 365 | 369 | PF00082 | 0.422 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.502 |
CLV_PCSK_FUR_1 | 429 | 433 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.703 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.443 |
CLV_PCSK_PC7_1 | 363 | 369 | PF00082 | 0.425 |
CLV_PCSK_PC7_1 | 420 | 426 | PF00082 | 0.507 |
CLV_PCSK_PC7_1 | 427 | 433 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.430 |
DEG_APCC_DBOX_1 | 152 | 160 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 419 | 427 | PF00400 | 0.515 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.652 |
DEG_SPOP_SBC_1 | 36 | 40 | PF00917 | 0.561 |
DEG_SPOP_SBC_1 | 397 | 401 | PF00917 | 0.627 |
DOC_CYCLIN_RxL_1 | 123 | 131 | PF00134 | 0.428 |
DOC_MAPK_gen_1 | 336 | 344 | PF00069 | 0.345 |
DOC_MAPK_gen_1 | 445 | 452 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 445 | 452 | PF00069 | 0.585 |
DOC_MAPK_NFAT4_5 | 337 | 345 | PF00069 | 0.339 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.346 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.482 |
DOC_USP7_UBL2_3 | 358 | 362 | PF12436 | 0.543 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 146 | 156 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 35 | 44 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.554 |
LIG_Actin_WH2_1 | 432 | 449 | PF00022 | 0.455 |
LIG_BIR_III_2 | 376 | 380 | PF00653 | 0.509 |
LIG_BRCT_BRCA1_1 | 246 | 250 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 39 | 43 | PF00533 | 0.690 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.599 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.438 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.429 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.396 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.438 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.521 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.597 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.608 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.488 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.478 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.428 |
LIG_IRF3_LxIS_1 | 204 | 211 | PF10401 | 0.445 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.503 |
LIG_MAD2 | 263 | 271 | PF02301 | 0.381 |
LIG_MLH1_MIPbox_1 | 246 | 250 | PF16413 | 0.380 |
LIG_NRBOX | 155 | 161 | PF00104 | 0.438 |
LIG_Pex14_2 | 274 | 278 | PF04695 | 0.428 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.427 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.538 |
LIG_RPA_C_Fungi | 46 | 58 | PF08784 | 0.433 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.235 |
LIG_SH2_CRK | 66 | 70 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 279 | 283 | PF00017 | 0.237 |
LIG_SH2_STAT3 | 326 | 329 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.506 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.407 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.700 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.262 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.276 |
LIG_TRAF2_1 | 409 | 412 | PF00917 | 0.649 |
LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.576 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.229 |
MOD_CDK_SPK_2 | 17 | 22 | PF00069 | 0.456 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.654 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.410 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.599 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.549 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.667 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.407 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.405 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.636 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.792 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.648 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.584 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.262 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.262 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.272 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.255 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.255 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.501 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.468 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.683 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.752 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.664 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.620 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.586 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.547 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.407 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.317 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.248 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.394 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.563 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.721 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.593 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.648 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.276 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.385 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.276 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.145 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.566 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.232 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.404 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.481 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.476 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.529 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.515 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.458 |
MOD_PK_1 | 402 | 408 | PF00069 | 0.461 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.512 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.392 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.295 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.518 |
MOD_PKA_2 | 401 | 407 | PF00069 | 0.585 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.533 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.262 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.383 |
MOD_Plk_1 | 402 | 408 | PF00069 | 0.554 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.576 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.276 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.387 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.435 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.590 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.669 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.262 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.587 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.515 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_1 | 330 | 335 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 431 | 436 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.498 |
TRG_ER_diArg_1 | 261 | 264 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 413 | 416 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.531 |
TRG_NLS_MonoCore_2 | 361 | 366 | PF00514 | 0.462 |
TRG_NLS_MonoExtC_3 | 416 | 422 | PF00514 | 0.619 |
TRG_NLS_MonoExtN_4 | 414 | 421 | PF00514 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4G3 | Leptomonas seymouri | 71% | 100% |
A0A0S4IXW1 | Bodo saltans | 43% | 100% |
A0A1X0P5K8 | Trypanosomatidae | 56% | 100% |
A0A3R7N6Y9 | Trypanosoma rangeli | 55% | 100% |
A0A3S7X9K0 | Leishmania donovani | 96% | 100% |
A4HN02 | Leishmania braziliensis | 84% | 100% |
A4IBM5 | Leishmania infantum | 96% | 100% |
C9ZZ09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9B6L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BY28 | Trypanosoma cruzi | 55% | 100% |