| 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 | yes | yes: 1, no: 4 |
| NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AC77
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006793 | phosphorus metabolic process | 3 | 6 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
| GO:0008152 | metabolic process | 1 | 6 |
| GO:0009987 | cellular process | 1 | 6 |
| GO:0016310 | phosphorylation | 5 | 6 |
| GO:0044237 | cellular metabolic process | 2 | 6 |
| GO:0005975 | carbohydrate metabolic process | 3 | 4 |
| GO:0044238 | primary metabolic process | 2 | 4 |
| GO:0071704 | organic substance metabolic process | 2 | 4 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 6 |
| GO:0009024 | tagatose-6-phosphate kinase activity | 5 | 5 |
| GO:0016301 | kinase activity | 4 | 6 |
| GO:0016740 | transferase activity | 2 | 6 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 201 | 205 | PF00656 | 0.456 |
| CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.456 |
| CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.463 |
| CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.466 |
| CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.478 |
| CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.466 |
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.256 |
| CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.260 |
| CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.256 |
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.257 |
| DEG_APCC_DBOX_1 | 183 | 191 | PF00400 | 0.520 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.438 |
| DEG_SPOP_SBC_1 | 373 | 377 | PF00917 | 0.587 |
| DOC_ANK_TNKS_1 | 359 | 366 | PF00023 | 0.477 |
| DOC_CKS1_1 | 259 | 264 | PF01111 | 0.456 |
| DOC_CYCLIN_RxL_1 | 68 | 77 | PF00134 | 0.379 |
| DOC_MAPK_gen_1 | 360 | 368 | PF00069 | 0.492 |
| DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.471 |
| DOC_MAPK_MEF2A_6 | 53 | 62 | PF00069 | 0.312 |
| DOC_MAPK_MEF2A_6 | 7 | 16 | PF00069 | 0.420 |
| DOC_PP1_SILK_1 | 243 | 248 | PF00149 | 0.520 |
| DOC_PP2B_LxvP_1 | 237 | 240 | PF13499 | 0.456 |
| DOC_PP2B_PxIxI_1 | 57 | 63 | PF00149 | 0.458 |
| DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.520 |
| DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.456 |
| DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.587 |
| DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.429 |
| DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.418 |
| DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.456 |
| DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.456 |
| DOC_WW_Pin1_4 | 306 | 311 | PF00397 | 0.456 |
| DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.520 |
| DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.471 |
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.332 |
| LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.491 |
| LIG_14-3-3_CanoR_1 | 40 | 49 | PF00244 | 0.476 |
| LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.560 |
| LIG_BRCT_BRCA1_1 | 109 | 113 | PF00533 | 0.448 |
| LIG_DLG_GKlike_1 | 8 | 15 | PF00625 | 0.420 |
| LIG_FHA_1 | 163 | 169 | PF00498 | 0.456 |
| LIG_FHA_1 | 272 | 278 | PF00498 | 0.456 |
| LIG_FHA_1 | 327 | 333 | PF00498 | 0.520 |
| LIG_FHA_1 | 70 | 76 | PF00498 | 0.359 |
| LIG_FHA_2 | 153 | 159 | PF00498 | 0.456 |
| LIG_FHA_2 | 161 | 167 | PF00498 | 0.456 |
| LIG_FHA_2 | 27 | 33 | PF00498 | 0.461 |
| LIG_FHA_2 | 328 | 334 | PF00498 | 0.520 |
| LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.520 |
| LIG_MAD2 | 276 | 284 | PF02301 | 0.520 |
| LIG_NRBOX | 11 | 17 | PF00104 | 0.422 |
| LIG_PDZ_Class_1 | 376 | 381 | PF00595 | 0.645 |
| LIG_PTB_Apo_2 | 63 | 70 | PF02174 | 0.430 |
| LIG_SH2_SRC | 325 | 328 | PF00017 | 0.456 |
| LIG_SH2_STAP1 | 268 | 272 | PF00017 | 0.548 |
| LIG_SH2_STAT3 | 268 | 271 | PF00017 | 0.520 |
| LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.520 |
| LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.456 |
| LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.472 |
| LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.456 |
| LIG_SH3_2 | 48 | 53 | PF14604 | 0.443 |
| LIG_SH3_3 | 141 | 147 | PF00018 | 0.520 |
| LIG_SH3_3 | 296 | 302 | PF00018 | 0.457 |
| LIG_SH3_3 | 304 | 310 | PF00018 | 0.420 |
| LIG_SH3_3 | 45 | 51 | PF00018 | 0.596 |
| LIG_SH3_3 | 59 | 65 | PF00018 | 0.340 |
| LIG_SUMO_SIM_anti_2 | 9 | 14 | PF11976 | 0.419 |
| LIG_SUMO_SIM_par_1 | 223 | 228 | PF11976 | 0.456 |
| LIG_SUMO_SIM_par_1 | 276 | 282 | PF11976 | 0.456 |
| LIG_SUMO_SIM_par_1 | 71 | 77 | PF11976 | 0.297 |
| LIG_TRFH_1 | 17 | 21 | PF08558 | 0.418 |
| LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.456 |
| MOD_CK1_1 | 162 | 168 | PF00069 | 0.520 |
| MOD_CK1_1 | 27 | 33 | PF00069 | 0.461 |
| MOD_CK2_1 | 160 | 166 | PF00069 | 0.547 |
| MOD_CK2_1 | 257 | 263 | PF00069 | 0.456 |
| MOD_CK2_1 | 327 | 333 | PF00069 | 0.520 |
| MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.256 |
| MOD_GlcNHglycan | 169 | 173 | PF01048 | 0.287 |
| MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.455 |
| MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.269 |
| MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.256 |
| MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.264 |
| MOD_GSK3_1 | 113 | 120 | PF00069 | 0.456 |
| MOD_GSK3_1 | 152 | 159 | PF00069 | 0.520 |
| MOD_GSK3_1 | 20 | 27 | PF00069 | 0.430 |
| MOD_GSK3_1 | 254 | 261 | PF00069 | 0.474 |
| MOD_GSK3_1 | 36 | 43 | PF00069 | 0.473 |
| MOD_GSK3_1 | 364 | 371 | PF00069 | 0.448 |
| MOD_GSK3_1 | 372 | 379 | PF00069 | 0.584 |
| MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.320 |
| MOD_N-GLC_2 | 99 | 101 | PF02516 | 0.256 |
| MOD_NEK2_1 | 113 | 118 | PF00069 | 0.520 |
| MOD_NEK2_1 | 24 | 29 | PF00069 | 0.449 |
| MOD_NEK2_1 | 69 | 74 | PF00069 | 0.374 |
| MOD_NEK2_2 | 114 | 119 | PF00069 | 0.429 |
| MOD_PIKK_1 | 156 | 162 | PF00454 | 0.520 |
| MOD_PKA_2 | 101 | 107 | PF00069 | 0.433 |
| MOD_PKA_2 | 114 | 120 | PF00069 | 0.456 |
| MOD_PKA_2 | 212 | 218 | PF00069 | 0.456 |
| MOD_Plk_1 | 160 | 166 | PF00069 | 0.520 |
| MOD_Plk_1 | 233 | 239 | PF00069 | 0.461 |
| MOD_Plk_1 | 8 | 14 | PF00069 | 0.420 |
| MOD_Plk_4 | 117 | 123 | PF00069 | 0.466 |
| MOD_Plk_4 | 241 | 247 | PF00069 | 0.468 |
| MOD_Plk_4 | 8 | 14 | PF00069 | 0.472 |
| MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.429 |
| MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.420 |
| MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.456 |
| MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.456 |
| MOD_ProDKin_1 | 306 | 312 | PF00069 | 0.456 |
| MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.520 |
| MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.466 |
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.315 |
| TRG_DiLeu_BaLyEn_6 | 55 | 60 | PF01217 | 0.606 |
| TRG_ER_diArg_1 | 359 | 361 | PF00400 | 0.553 |
| TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.421 |
| TRG_NES_CRM1_1 | 271 | 282 | PF08389 | 0.520 |
| TRG_Pf-PMV_PEXEL_1 | 360 | 364 | PF00026 | 0.482 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I6N7 | Leptomonas seymouri | 69% | 100% |
| A0A3S5H4X6 | Leishmania donovani | 94% | 100% |
| A2RGF2 | Streptococcus pyogenes serotype M5 (strain Manfredo) | 27% | 100% |
| A3CPH5 | Streptococcus sanguinis (strain SK36) | 27% | 100% |
| A5IUY2 | Staphylococcus aureus (strain JH9) | 28% | 100% |
| A6QJ37 | Staphylococcus aureus (strain Newman) | 28% | 100% |
| A6U3S3 | Staphylococcus aureus (strain JH1) | 28% | 100% |
| A7X575 | Staphylococcus aureus (strain Mu3 / ATCC 700698) | 28% | 100% |
| A8YYG0 | Staphylococcus aureus (strain USA300 / TCH1516) | 28% | 100% |
| B1IBZ5 | Streptococcus pneumoniae (strain Hungary19A-6) | 30% | 100% |
| B2IPT7 | Streptococcus pneumoniae (strain CGSP14) | 30% | 100% |
| B5E4T0 | Streptococcus pneumoniae serotype 19F (strain G54) | 29% | 100% |
| B5XII4 | Streptococcus pyogenes serotype M49 (strain NZ131) | 27% | 100% |
| B8ZQ64 | Streptococcus pneumoniae (strain ATCC 700669 / Spain 23F-1) | 30% | 100% |
| B9DU93 | Streptococcus uberis (strain ATCC BAA-854 / 0140J) | 28% | 100% |
| C1C7G0 | Streptococcus pneumoniae (strain 70585) | 30% | 100% |
| C1CEF2 | Streptococcus pneumoniae (strain JJA) | 30% | 100% |
| C1CKT7 | Streptococcus pneumoniae (strain P1031) | 29% | 100% |
| C1CRA6 | Streptococcus pneumoniae (strain Taiwan19F-14) | 29% | 100% |
| D4GYE6 | Haloferax volcanii (strain ATCC 29605 / DSM 3757 / JCM 8879 / NBRC 14742 / NCIMB 2012 / VKM B-1768 / DS2) | 27% | 100% |
| E9AHA4 | Leishmania infantum | 94% | 100% |
| O31714 | Bacillus subtilis (strain 168) | 27% | 100% |
| P06999 | Escherichia coli (strain K12) | 25% | 100% |
| P0A0B8 | Staphylococcus aureus (strain MW2) | 28% | 100% |
| P0A0B9 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 28% | 100% |
| P0AEW9 | Escherichia coli (strain K12) | 25% | 100% |
| P0AEX0 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 25% | 100% |
| P0AEX1 | Escherichia coli O157:H7 | 25% | 100% |
| P0AEX2 | Shigella flexneri | 25% | 100% |
| P0DC12 | Streptococcus pyogenes serotype M3 (strain ATCC BAA-595 / MGAS315) | 28% | 100% |
| P0DC13 | Streptococcus pyogenes serotype M3 (strain SSI-1) | 28% | 100% |
| P23391 | Lactococcus lactis subsp. lactis | 27% | 100% |
| P26421 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 28% | 100% |
| P44330 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 24% | 100% |
| P65698 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 28% | 100% |
| P65699 | Staphylococcus aureus (strain N315) | 28% | 100% |
| P75038 | Mycoplasma pneumoniae (strain ATCC 29342 / M129 / Subtype 1) | 26% | 100% |
| P9WID2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 26% | 100% |
| P9WID3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 26% | 100% |
| Q04KC3 | Streptococcus pneumoniae serotype 2 (strain D39 / NCTC 7466) | 30% | 100% |
| Q1J4Q3 | Streptococcus pyogenes serotype M4 (strain MGAS10750) | 27% | 100% |
| Q1J9U8 | Streptococcus pyogenes serotype M12 (strain MGAS2096) | 28% | 100% |
| Q1JEY9 | Streptococcus pyogenes serotype M2 (strain MGAS10270) | 27% | 100% |
| Q1JJZ7 | Streptococcus pyogenes serotype M12 (strain MGAS9429) | 28% | 100% |
| Q2FET9 | Staphylococcus aureus (strain USA300) | 28% | 100% |
| Q2YYJ5 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 28% | 100% |
| Q3JZ20 | Streptococcus agalactiae serotype Ia (strain ATCC 27591 / A909 / CDC SS700) | 27% | 100% |
| Q48RC4 | Streptococcus pyogenes serotype M28 (strain MGAS6180) | 27% | 100% |
| Q4L872 | Staphylococcus haemolyticus (strain JCSC1435) | 25% | 100% |
| Q4Q9J4 | Leishmania major | 100% | 100% |
| Q5HE12 | Staphylococcus aureus (strain COL) | 28% | 100% |
| Q5HM37 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 24% | 100% |
| Q5X9Y3 | Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) | 27% | 100% |
| Q6G7C1 | Staphylococcus aureus (strain MSSA476) | 28% | 100% |
| Q6GEN6 | Staphylococcus aureus (strain MRSA252) | 28% | 100% |
| Q833W9 | Enterococcus faecalis (strain ATCC 700802 / V583) | 25% | 100% |
| Q8CRJ4 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 24% | 100% |
| Q8DPP1 | Streptococcus pneumoniae (strain ATCC BAA-255 / R6) | 30% | 100% |
| Q8DXC2 | Streptococcus agalactiae serotype V (strain ATCC BAA-611 / 2603 V/R) | 27% | 100% |
| Q8E346 | Streptococcus agalactiae serotype III (strain NEM316) | 27% | 100% |
| Q8E4R7 | Streptococcus agalactiae serotype III (strain NEM316) | 26% | 100% |
| Q8NZD9 | Streptococcus pyogenes serotype M18 (strain MGAS8232) | 27% | 100% |
| Q8XNK5 | Clostridium perfringens (strain 13 / Type A) | 24% | 100% |
| Q97QL2 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 29% | 100% |
| Q99Y14 | Streptococcus pyogenes serotype M1 | 28% | 100% |
| Q9KM71 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 22% | 100% |