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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9B1Q2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 364 | 368 | PF00656 | 0.671 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.712 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.657 |
DOC_CKS1_1 | 8 | 13 | PF01111 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 146 | PF00134 | 0.531 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.608 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.535 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.679 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.645 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.682 |
DOC_USP7_UBL2_3 | 280 | 284 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.755 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.768 |
LIG_BIR_III_4 | 367 | 371 | PF00653 | 0.556 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.681 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.625 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.514 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.474 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.679 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.546 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.643 |
LIG_LIR_Gen_1 | 121 | 130 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.470 |
LIG_PDZ_Class_1 | 378 | 383 | PF00595 | 0.672 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.646 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.674 |
LIG_SH3_4 | 280 | 287 | PF00018 | 0.658 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.463 |
LIG_UBA3_1 | 123 | 131 | PF00899 | 0.469 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.680 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.692 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.677 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.704 |
MOD_CK2_1 | 114 | 120 | PF00069 | 0.649 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.679 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.545 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.545 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.690 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.559 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.652 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.756 |
MOD_Cter_Amidation | 154 | 157 | PF01082 | 0.655 |
MOD_Cter_Amidation | 207 | 210 | PF01082 | 0.693 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.763 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.701 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.540 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.491 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.787 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.542 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.678 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.724 |
MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.689 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.649 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.548 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.671 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.754 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.707 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.654 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.688 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.585 |
MOD_LATS_1 | 60 | 66 | PF00433 | 0.636 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.562 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.513 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.543 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.469 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.690 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.596 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.526 |
MOD_PIKK_1 | 211 | 217 | PF00454 | 0.669 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.679 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.690 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.657 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.682 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.479 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.719 |
MOD_PKB_1 | 197 | 205 | PF00069 | 0.539 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.632 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.601 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.554 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.756 |
MOD_SUMO_rev_2 | 118 | 124 | PF00179 | 0.595 |
MOD_SUMO_rev_2 | 324 | 333 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 7 | 17 | PF00179 | 0.504 |
TRG_DiLeu_BaEn_2 | 119 | 125 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.536 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.667 |
TRG_ER_KDEL_1 | 380 | 383 | PF00810 | 0.667 |
TRG_NLS_MonoExtC_3 | 155 | 160 | PF00514 | 0.649 |
TRG_NLS_MonoExtN_4 | 154 | 160 | PF00514 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IJY9 | Leishmania donovani | 73% | 100% |
A4HJ85 | Leishmania braziliensis | 35% | 100% |
A4I6M9 | Leishmania infantum | 74% | 100% |
Q4Q6F8 | Leishmania major | 71% | 100% |