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: 20 |
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: 2, no: 13 |
NetGPI | no | yes: 0, no: 15 |
Related structures:
AlphaFold database: A4HYK3
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
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_C14_Caspase3-7 | 143 | 147 | PF00656 | 0.400 |
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.393 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.692 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.692 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.582 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.529 |
DEG_SCF_FBW7_1 | 201 | 207 | PF00400 | 0.423 |
DOC_ANK_TNKS_1 | 216 | 223 | PF00023 | 0.306 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.427 |
DOC_PP1_RVXF_1 | 152 | 158 | PF00149 | 0.306 |
DOC_PP1_RVXF_1 | 230 | 236 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 382 | 388 | PF00149 | 0.672 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.618 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.539 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.624 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.483 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.421 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.355 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.504 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.507 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.424 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.326 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 411 | 415 | PF02991 | 0.609 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 182 | 192 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 362 | 370 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.488 |
LIG_Pex14_2 | 235 | 239 | PF04695 | 0.336 |
LIG_Pex14_2 | 408 | 412 | PF04695 | 0.474 |
LIG_Pex14_2 | 74 | 78 | PF04695 | 0.413 |
LIG_REV1ctd_RIR_1 | 165 | 174 | PF16727 | 0.409 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.601 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.374 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.455 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.574 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.360 |
LIG_TYR_ITSM | 90 | 97 | PF00017 | 0.502 |
LIG_WRC_WIRS_1 | 409 | 414 | PF05994 | 0.505 |
MOD_CDK_SPxK_1 | 438 | 444 | PF00069 | 0.598 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.621 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.435 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.596 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.433 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.430 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.531 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.769 |
MOD_GlcNHglycan | 394 | 399 | PF01048 | 0.563 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.443 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.451 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.510 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.658 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.568 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.525 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.443 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.503 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.457 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.389 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.498 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.598 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.575 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.388 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.537 |
MOD_PKA_1 | 197 | 203 | PF00069 | 0.522 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.536 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.470 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.415 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.400 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.504 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.324 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.506 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.639 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.421 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.761 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.598 |
MOD_SUMO_for_1 | 123 | 126 | PF00179 | 0.330 |
TRG_DiLeu_BaEn_4 | 64 | 70 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.493 |
TRG_ER_diArg_1 | 196 | 198 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.695 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S2 | Leptomonas seymouri | 78% | 100% |
A0A0S4JFV2 | Bodo saltans | 51% | 100% |
A0A1X0NX05 | Trypanosomatidae | 60% | 100% |
A0A3S7WVR3 | Leishmania donovani | 100% | 100% |
A0A3S7X3U7 | Leishmania donovani | 31% | 100% |
A0A422N7V9 | Trypanosoma rangeli | 58% | 100% |
A4HBI1 | Leishmania braziliensis | 89% | 100% |
A4HIR9 | Leishmania braziliensis | 31% | 100% |
A4I615 | Leishmania infantum | 31% | 100% |
C9ZHV2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AUF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q6V8 | Leishmania major | 31% | 100% |
Q4QD31 | Leishmania major | 96% | 100% |
V5C0D1 | Trypanosoma cruzi | 59% | 100% |