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: A4I5N5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.615 |
CLV_PCSK_FUR_1 | 123 | 127 | PF00082 | 0.719 |
CLV_PCSK_FUR_1 | 152 | 156 | PF00082 | 0.641 |
CLV_PCSK_FUR_1 | 68 | 72 | PF00082 | 0.703 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.627 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.613 |
DEG_SCF_FBW7_1 | 111 | 116 | PF00400 | 0.711 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.555 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.755 |
DOC_MAPK_DCC_7 | 196 | 204 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 196 | 204 | PF00069 | 0.628 |
DOC_MAPK_MEF2A_6 | 244 | 253 | PF00069 | 0.632 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.630 |
DOC_USP7_UBL2_3 | 205 | 209 | PF12436 | 0.471 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.708 |
LIG_14-3-3_CanoR_1 | 114 | 122 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 133 | 142 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.540 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.620 |
LIG_deltaCOP1_diTrp_1 | 243 | 248 | PF00928 | 0.618 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.543 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.483 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.642 |
LIG_LIR_Gen_1 | 18 | 24 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 302 | 311 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 18 | 23 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 302 | 306 | PF02991 | 0.485 |
LIG_SH2_PTP2 | 127 | 130 | PF00017 | 0.660 |
LIG_SH2_SRC | 127 | 130 | PF00017 | 0.663 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.685 |
LIG_SH3_1 | 278 | 284 | PF00018 | 0.608 |
LIG_SH3_2 | 200 | 205 | PF14604 | 0.647 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.715 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.711 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.577 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.544 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.516 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.698 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.669 |
LIG_SH3_4 | 192 | 199 | PF00018 | 0.658 |
LIG_SH3_4 | 205 | 212 | PF00018 | 0.676 |
LIG_SUMO_SIM_par_1 | 273 | 279 | PF11976 | 0.673 |
LIG_WW_2 | 200 | 203 | PF00397 | 0.494 |
MOD_CDK_SPK_2 | 109 | 114 | PF00069 | 0.678 |
MOD_CDK_SPxK_1 | 294 | 300 | PF00069 | 0.552 |
MOD_CDK_SPxK_1 | 62 | 68 | PF00069 | 0.730 |
MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.609 |
MOD_CDK_SPxxK_3 | 294 | 301 | PF00069 | 0.514 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.690 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.615 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.731 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.652 |
MOD_Cter_Amidation | 253 | 256 | PF01082 | 0.512 |
MOD_Cter_Amidation | 290 | 293 | PF01082 | 0.669 |
MOD_Cter_Amidation | 68 | 71 | PF01082 | 0.624 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.730 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.665 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.589 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.392 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.608 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.708 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.662 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.547 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.624 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.713 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.636 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.557 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.610 |
MOD_NEK2_2 | 15 | 20 | PF00069 | 0.499 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.650 |
MOD_PK_1 | 162 | 168 | PF00069 | 0.735 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.614 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.593 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.642 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.552 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.545 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.752 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.754 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.620 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.655 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.486 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.674 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.668 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.673 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.636 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.717 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.578 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.714 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 152 | 155 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.646 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.540 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 94 | 96 | PF00400 | 0.656 |
TRG_Pf-PMV_PEXEL_1 | 6 | 10 | PF00026 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P913 | Leptomonas seymouri | 62% | 100% |
A0A1X0P1U3 | Trypanosomatidae | 31% | 100% |
A0A3Q8IFW1 | Leishmania donovani | 100% | 100% |
A0A422P3E4 | Trypanosoma rangeli | 34% | 100% |
A4HID8 | Leishmania braziliensis | 77% | 100% |
C9ZR04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B0X9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q787 | Leishmania major | 93% | 100% |
V5BYT6 | Trypanosoma cruzi | 32% | 99% |