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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q207
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.562 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.644 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.773 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.728 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.667 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.759 |
DEG_SPOP_SBC_1 | 197 | 201 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 64 | 68 | PF00917 | 0.654 |
DOC_MAPK_DCC_7 | 242 | 251 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.520 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.397 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.656 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.512 |
LIG_14-3-3_CanoR_1 | 133 | 140 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 209 | 215 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 62 | 71 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 85 | 93 | PF00244 | 0.766 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.621 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.649 |
LIG_FHA_2 | 199 | 205 | PF00498 | 0.614 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.639 |
LIG_MYND_3 | 246 | 250 | PF01753 | 0.598 |
LIG_PCNA_yPIPBox_3 | 222 | 236 | PF02747 | 0.514 |
LIG_SH2_SRC | 108 | 111 | PF00017 | 0.563 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.601 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.555 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.641 |
LIG_SUMO_SIM_par_1 | 90 | 96 | PF11976 | 0.641 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.711 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.673 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.667 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.634 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.708 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.651 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.690 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.500 |
MOD_CK2_1 | 210 | 216 | PF00069 | 0.331 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.660 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.646 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.696 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.667 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.649 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.728 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.480 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.765 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.630 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.616 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.767 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.666 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.673 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.662 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.675 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.686 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.646 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.695 |
MOD_N-GLC_1 | 141 | 146 | PF02516 | 0.576 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.602 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.612 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.605 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.601 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.644 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.536 |
MOD_NEK2_2 | 22 | 27 | PF00069 | 0.687 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.618 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.676 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.609 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.573 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.529 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.370 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.766 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.654 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.508 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.681 |
TRG_NES_CRM1_1 | 239 | 250 | PF08389 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 85 | 90 | PF00026 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFQ8 | Leptomonas seymouri | 37% | 89% |
A0A3S7XAG1 | Leishmania donovani | 90% | 100% |
A4HNS9 | Leishmania braziliensis | 76% | 100% |
A4ICR5 | Leishmania infantum | 90% | 100% |
E9ASI9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |