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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9B141
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.355 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.708 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.426 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.784 |
DOC_CYCLIN_RxL_1 | 160 | 167 | PF00134 | 0.658 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.733 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.519 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.714 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.553 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.717 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.447 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.643 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 35 | 42 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.321 |
LIG_MYND_1 | 127 | 131 | PF01753 | 0.769 |
LIG_PCNA_yPIPBox_3 | 163 | 177 | PF02747 | 0.574 |
LIG_PDZ_Class_2 | 289 | 294 | PF00595 | 0.686 |
LIG_PTB_Apo_2 | 176 | 183 | PF02174 | 0.569 |
LIG_PTB_Phospho_1 | 176 | 182 | PF10480 | 0.570 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.643 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.508 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.681 |
MOD_CDC14_SPxK_1 | 85 | 88 | PF00782 | 0.777 |
MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.679 |
MOD_CDK_SPxK_1 | 263 | 269 | PF00069 | 0.698 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.783 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.635 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.637 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.679 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.478 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.594 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.472 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.570 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.539 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.527 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.506 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.587 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.631 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.651 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.724 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.559 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.655 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.522 |
MOD_GlcNHglycan | 96 | 100 | PF01048 | 0.665 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.620 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.680 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.591 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.568 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.633 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.640 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.651 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.709 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.601 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.711 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.642 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.572 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.508 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.640 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.355 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.503 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.487 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.434 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.398 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.698 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.660 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.671 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.698 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.679 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.693 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.462 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.487 |
MOD_SUMO_for_1 | 38 | 41 | PF00179 | 0.173 |
MOD_SUMO_rev_2 | 238 | 245 | PF00179 | 0.510 |
TRG_AP2beta_CARGO_1 | 180 | 190 | PF09066 | 0.472 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T5 | Leptomonas seymouri | 60% | 92% |
A0A1X0P1K4 | Trypanosomatidae | 42% | 100% |
A0A3Q8IG02 | Leishmania donovani | 95% | 100% |
A0A422NLQ1 | Trypanosoma rangeli | 39% | 100% |
A4HIK1 | Leishmania braziliensis | 82% | 100% |
A4I5U6 | Leishmania infantum | 95% | 100% |
C9ZR67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
Q4Q725 | Leishmania major | 93% | 100% |
V5BX71 | Trypanosoma cruzi | 44% | 100% |