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: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9ATY9
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0016301 | kinase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.423 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.468 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.312 |
CLV_PCSK_PC7_1 | 197 | 203 | PF00082 | 0.340 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.449 |
DEG_APCC_DBOX_1 | 175 | 183 | PF00400 | 0.435 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.403 |
DOC_CYCLIN_RxL_1 | 98 | 110 | PF00134 | 0.507 |
DOC_MAPK_gen_1 | 98 | 107 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.454 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.492 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 400 | 409 | PF00244 | 0.512 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.752 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.674 |
LIG_CSL_BTD_1 | 217 | 220 | PF09270 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 439 | 444 | PF00928 | 0.267 |
LIG_eIF4E_1 | 235 | 241 | PF01652 | 0.354 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.349 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.366 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.480 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.505 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.406 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.610 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.469 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.695 |
LIG_HCF-1_HBM_1 | 232 | 235 | PF13415 | 0.512 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.458 |
LIG_LIR_Apic_2 | 216 | 221 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.426 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.484 |
LIG_Rb_pABgroove_1 | 225 | 233 | PF01858 | 0.513 |
LIG_SH2_NCK_1 | 235 | 239 | PF00017 | 0.521 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.355 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 428 | 431 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.266 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.715 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.565 |
LIG_SH3_3 | 242 | 248 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 178 | 184 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 410 | 416 | PF11976 | 0.544 |
LIG_SxIP_EBH_1 | 16 | 28 | PF03271 | 0.463 |
LIG_WW_3 | 373 | 377 | PF00397 | 0.366 |
MOD_CDC14_SPxK_1 | 373 | 376 | PF00782 | 0.374 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.554 |
MOD_CDK_SPxK_1 | 370 | 376 | PF00069 | 0.614 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.350 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.605 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.497 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.635 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.524 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.494 |
MOD_CMANNOS | 251 | 254 | PF00535 | 0.556 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.512 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.459 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.658 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.502 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.383 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.501 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.719 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.515 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.433 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.703 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.583 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.492 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.467 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.581 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.470 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.509 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.569 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.376 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.361 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.392 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.549 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.361 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.551 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.610 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.540 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.299 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.493 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.396 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.664 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.678 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.522 |
MOD_SUMO_for_1 | 387 | 390 | PF00179 | 0.550 |
MOD_SUMO_for_1 | 405 | 408 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 86 | 93 | PF00179 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ4 | Leptomonas seymouri | 36% | 98% |
A0A1X0P061 | Trypanosomatidae | 23% | 100% |
A0A3Q8ILN7 | Leishmania donovani | 85% | 100% |
A0A422NKD5 | Trypanosoma rangeli | 25% | 100% |
A4HQ70 | Leishmania braziliensis | 72% | 100% |
A4IDW8 | Leishmania infantum | 86% | 100% |
D0A449 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4Q0K7 | Leishmania major | 85% | 100% |