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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AJZ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.518 |
CLV_PCSK_FUR_1 | 101 | 105 | PF00082 | 0.630 |
CLV_PCSK_FUR_1 | 130 | 134 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 218 | 226 | PF00400 | 0.528 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.418 |
DEG_SCF_FBW7_1 | 138 | 145 | PF00400 | 0.620 |
DOC_MAPK_gen_1 | 130 | 140 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 266 | 275 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 356 | 366 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 372 | 378 | PF00069 | 0.330 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.529 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 132 | 137 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 305 | 309 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 90 | 98 | PF00244 | 0.528 |
LIG_Actin_WH2_2 | 165 | 180 | PF00022 | 0.608 |
LIG_Actin_WH2_2 | 341 | 358 | PF00022 | 0.466 |
LIG_eIF4E_1 | 67 | 73 | PF01652 | 0.567 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.648 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.566 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.417 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.416 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.675 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.642 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.541 |
LIG_GBD_Chelix_1 | 233 | 241 | PF00786 | 0.445 |
LIG_LIR_Gen_1 | 62 | 73 | PF02991 | 0.687 |
LIG_LIR_Nem_3 | 319 | 324 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 365 | 369 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.587 |
LIG_PCNA_yPIPBox_3 | 274 | 283 | PF02747 | 0.373 |
LIG_SH2_CRK | 280 | 284 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.703 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.512 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.444 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.614 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.811 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.806 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.684 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.667 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.439 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.392 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.565 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.642 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.595 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.646 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.473 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.640 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.765 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.728 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.679 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.550 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.764 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.696 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.560 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.553 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.660 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.644 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.563 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.656 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.620 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.578 |
MOD_NEK2_2 | 3 | 8 | PF00069 | 0.513 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.548 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.638 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.530 |
MOD_PKA_1 | 132 | 138 | PF00069 | 0.508 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.679 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.621 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.556 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.566 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.642 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.574 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.576 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.664 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.611 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.656 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.621 |
MOD_PKB_1 | 11 | 19 | PF00069 | 0.509 |
MOD_PKB_1 | 130 | 138 | PF00069 | 0.507 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.613 |
MOD_Plk_2-3 | 204 | 210 | PF00069 | 0.620 |
MOD_Plk_2-3 | 57 | 63 | PF00069 | 0.387 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.374 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.528 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.441 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.471 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.747 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.577 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.566 |
MOD_SUMO_rev_2 | 174 | 180 | PF00179 | 0.480 |
TRG_DiLeu_BaEn_4 | 163 | 169 | PF01217 | 0.566 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 278 | 283 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 280 | 283 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 130 | 133 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVL6 | Leptomonas seymouri | 36% | 94% |
A0A3S5H580 | Leishmania donovani | 84% | 89% |
A4H3T5 | Leishmania braziliensis | 64% | 100% |
A4HS10 | Leishmania infantum | 84% | 89% |
E9ACP7 | Leishmania major | 83% | 100% |
V5BDS0 | Trypanosoma cruzi | 24% | 91% |