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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3S7X9G6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.573 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.456 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.662 |
DEG_SPOP_SBC_1 | 361 | 365 | PF00917 | 0.667 |
DOC_CYCLIN_RxL_1 | 90 | 97 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 321 | 331 | PF00069 | 0.494 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.640 |
DOC_SPAK_OSR1_1 | 16 | 20 | PF12202 | 0.456 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.415 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 107 | 112 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 342 | 359 | PF00022 | 0.517 |
LIG_AP2alpha_1 | 133 | 137 | PF02296 | 0.474 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.645 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.783 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.379 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.432 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.769 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.549 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.584 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.428 |
LIG_LIR_Apic_2 | 26 | 32 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 236 | 246 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 236 | 241 | PF02991 | 0.404 |
LIG_NRBOX | 274 | 280 | PF00104 | 0.446 |
LIG_NRBOX | 90 | 96 | PF00104 | 0.521 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.433 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.528 |
LIG_SH2_SRC | 312 | 315 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.525 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.731 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.619 |
LIG_SUMO_SIM_anti_2 | 326 | 333 | PF11976 | 0.523 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.763 |
LIG_TRAF2_1 | 373 | 376 | PF00917 | 0.763 |
LIG_TRFH_1 | 111 | 115 | PF08558 | 0.415 |
LIG_UBA3_1 | 278 | 282 | PF00899 | 0.414 |
LIG_UBA3_1 | 66 | 73 | PF00899 | 0.457 |
LIG_UBA3_1 | 74 | 81 | PF00899 | 0.447 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.623 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.586 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.718 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.588 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.677 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.650 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.783 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.595 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.567 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.566 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.567 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.545 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.673 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.762 |
MOD_GlcNHglycan | 304 | 308 | PF01048 | 0.430 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.670 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.657 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.584 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.571 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.679 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.591 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.636 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.441 |
MOD_LATS_1 | 268 | 274 | PF00433 | 0.495 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.592 |
MOD_N-GLC_1 | 19 | 24 | PF02516 | 0.624 |
MOD_N-GLC_2 | 147 | 149 | PF02516 | 0.544 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.576 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.558 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.411 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.497 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.507 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.707 |
MOD_PIKK_1 | 340 | 346 | PF00454 | 0.501 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.620 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.392 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.460 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.529 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.410 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.500 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.787 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.629 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.466 |
MOD_SUMO_rev_2 | 350 | 359 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 77 | 83 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 327 | 332 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 73 | 77 | PF00026 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 93 | 97 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBE1 | Leptomonas seymouri | 67% | 100% |
A0A0S4JHH3 | Bodo saltans | 47% | 100% |
A0A1X0P5G2 | Trypanosomatidae | 56% | 100% |
A0A422P2T5 | Trypanosoma rangeli | 56% | 100% |
A4HMW4 | Leishmania braziliensis | 81% | 100% |
A4IBI5 | Leishmania infantum | 98% | 100% |
C9ZZ56 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AFC1 | Leishmania major | 91% | 100% |
E9B6H6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5BD06 | Trypanosoma cruzi | 59% | 100% |