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: 3, no: 3 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APN8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006397 | mRNA processing | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004651 | polynucleotide 5'-phosphatase activity | 6 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.666 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.379 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 376 | 378 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.468 |
DEG_SCF_FBW7_1 | 201 | 207 | PF00400 | 0.534 |
DEG_SPOP_SBC_1 | 14 | 18 | PF00917 | 0.460 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.447 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.346 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.537 |
DOC_CKS1_1 | 336 | 341 | PF01111 | 0.678 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.693 |
DOC_CYCLIN_yCln2_LP_2 | 336 | 342 | PF00134 | 0.601 |
DOC_MAPK_FxFP_2 | 11 | 14 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 110 | 118 | PF00069 | 0.695 |
DOC_MAPK_gen_1 | 229 | 238 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 110 | 118 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 169 | 176 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 253 | 261 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 95 | 102 | PF00069 | 0.573 |
DOC_PP1_RVXF_1 | 295 | 302 | PF00149 | 0.591 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.691 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.614 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 52 | 56 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.526 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 284 | 289 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 350 | 360 | PF00244 | 0.626 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.456 |
LIG_CtBP_PxDLS_1 | 258 | 262 | PF00389 | 0.668 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.476 |
LIG_eIF4E_2 | 302 | 308 | PF01652 | 0.612 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.662 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.480 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.643 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.509 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.637 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.548 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.560 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.532 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.813 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.611 |
LIG_GBD_Chelix_1 | 76 | 84 | PF00786 | 0.466 |
LIG_LIR_Apic_2 | 298 | 304 | PF02991 | 0.583 |
LIG_LIR_Apic_2 | 8 | 14 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 309 | 317 | PF02991 | 0.660 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.502 |
LIG_Pex14_1 | 375 | 379 | PF04695 | 0.486 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.724 |
LIG_SH2_CRK | 213 | 217 | PF00017 | 0.683 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.585 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.682 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.723 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.687 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.264 |
LIG_SUMO_SIM_anti_2 | 162 | 167 | PF11976 | 0.440 |
LIG_SUMO_SIM_anti_2 | 221 | 226 | PF11976 | 0.571 |
LIG_SUMO_SIM_anti_2 | 37 | 45 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.638 |
LIG_SUMO_SIM_par_1 | 354 | 363 | PF11976 | 0.458 |
LIG_WW_3 | 410 | 414 | PF00397 | 0.543 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.510 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.456 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.494 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.739 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.639 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.719 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.575 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.588 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.477 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.494 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.445 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.595 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.665 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.475 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.584 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.617 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.403 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.505 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.590 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.470 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.562 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.294 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.460 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.693 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.465 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.574 |
MOD_NEK2_2 | 405 | 410 | PF00069 | 0.717 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.604 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.578 |
MOD_PK_1 | 101 | 107 | PF00069 | 0.575 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.500 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.522 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.735 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.472 |
MOD_PKB_1 | 273 | 281 | PF00069 | 0.533 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.484 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.718 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.575 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.653 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.522 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.750 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.655 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.437 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.676 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.522 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.700 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.445 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.527 |
MOD_SUMO_rev_2 | 226 | 231 | PF00179 | 0.474 |
TRG_DiLeu_BaEn_1 | 433 | 438 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 140 | 145 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.715 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.655 |
TRG_NES_CRM1_1 | 164 | 179 | PF08389 | 0.348 |
TRG_NES_CRM1_1 | 70 | 85 | PF08389 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 131 | 135 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 284 | 289 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3D6 | Leptomonas seymouri | 38% | 100% |
A0A3Q8ID33 | Leishmania donovani | 88% | 100% |
A4H7K3 | Leishmania braziliensis | 78% | 100% |
A4HVY6 | Leishmania infantum | 88% | 100% |
Q4QFU1 | Leishmania major | 87% | 100% |