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: A4IDW8
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 | 410 | 414 | PF00656 | 0.648 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.651 |
CLV_PCSK_FUR_1 | 330 | 334 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.486 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.444 |
DEG_APCC_DBOX_1 | 175 | 183 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.480 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.398 |
DOC_CYCLIN_RxL_1 | 98 | 110 | PF00134 | 0.505 |
DOC_MAPK_JIP1_4 | 12 | 18 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.402 |
DOC_PP2B_PxIxI_1 | 130 | 136 | PF00149 | 0.385 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 330 | 338 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.404 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.745 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.667 |
LIG_CSL_BTD_1 | 217 | 220 | PF09270 | 0.511 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.314 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.394 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.642 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.466 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.392 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.586 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.543 |
LIG_HCF-1_HBM_1 | 232 | 235 | PF13415 | 0.523 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 216 | 221 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.425 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.431 |
LIG_Rb_pABgroove_1 | 225 | 233 | PF01858 | 0.494 |
LIG_SH2_NCK_1 | 235 | 239 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.614 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.715 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 410 | 420 | PF11976 | 0.509 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.412 |
LIG_SxIP_EBH_1 | 16 | 28 | PF03271 | 0.460 |
MOD_CDK_SPK_2 | 7 | 12 | PF00069 | 0.446 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.505 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.657 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.617 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.341 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.483 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.523 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.627 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.483 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.484 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.537 |
MOD_CMANNOS | 251 | 254 | PF00535 | 0.533 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.530 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.431 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.657 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.462 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.450 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.481 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.714 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.525 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.705 |
MOD_LATS_1 | 407 | 413 | PF00433 | 0.565 |
MOD_LATS_1 | 57 | 63 | PF00433 | 0.308 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.502 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.466 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.490 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.490 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.324 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.512 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.510 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.574 |
MOD_PK_1 | 59 | 65 | PF00069 | 0.367 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.325 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.561 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.430 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.475 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.583 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.555 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.524 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.484 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.485 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.405 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.549 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.392 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.629 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.681 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 387 | 390 | PF00179 | 0.532 |
MOD_SUMO_for_1 | 405 | 408 | PF00179 | 0.561 |
MOD_SUMO_rev_2 | 86 | 93 | PF00179 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 175 | 180 | PF01217 | 0.352 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ4 | Leptomonas seymouri | 36% | 96% |
A0A1X0P061 | Trypanosomatidae | 24% | 100% |
A0A3Q8ILN7 | Leishmania donovani | 99% | 100% |
A0A422NKD5 | Trypanosoma rangeli | 26% | 100% |
A4HQ70 | Leishmania braziliensis | 73% | 100% |
E9ATY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q0K7 | Leishmania major | 92% | 100% |
V5BNR2 | Trypanosoma cruzi | 27% | 100% |