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: E9AJZ5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.675 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.625 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.649 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.669 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.822 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.572 |
DEG_APCC_DBOX_1 | 124 | 132 | PF00400 | 0.520 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.643 |
DOC_CKS1_1 | 219 | 224 | PF01111 | 0.716 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.746 |
DOC_CKS1_1 | 281 | 286 | PF01111 | 0.537 |
DOC_MAPK_RevD_3 | 202 | 216 | PF00069 | 0.689 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.353 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.665 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 273 | 281 | PF00244 | 0.811 |
LIG_BIR_III_2 | 15 | 19 | PF00653 | 0.450 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.684 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.638 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.569 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.652 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.459 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.349 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.674 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.533 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.476 |
LIG_Integrin_RGD_1 | 258 | 260 | PF01839 | 0.725 |
LIG_LIR_Gen_1 | 146 | 157 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.514 |
LIG_NRBOX | 127 | 133 | PF00104 | 0.567 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.672 |
LIG_SH2_SRC | 207 | 210 | PF00017 | 0.634 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 59 | 63 | PF00017 | 0.521 |
LIG_SH3_1 | 216 | 222 | PF00018 | 0.657 |
LIG_SH3_2 | 206 | 211 | PF14604 | 0.768 |
LIG_SH3_3 | 203 | 209 | PF00018 | 0.652 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.654 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.834 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.584 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.660 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.532 |
LIG_Sin3_3 | 53 | 60 | PF02671 | 0.629 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 42 | 48 | PF11976 | 0.531 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.473 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.472 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.619 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.686 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.559 |
LIG_TYR_ITIM | 212 | 217 | PF00017 | 0.693 |
LIG_UBA3_1 | 326 | 334 | PF00899 | 0.629 |
MOD_CDK_SPxK_1 | 297 | 303 | PF00069 | 0.723 |
MOD_CDK_SPxxK_3 | 266 | 273 | PF00069 | 0.741 |
MOD_CDK_SPxxK_3 | 316 | 323 | PF00069 | 0.749 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.654 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.563 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.839 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.553 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.393 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.534 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.556 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.662 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.482 |
MOD_DYRK1A_RPxSP_1 | 297 | 301 | PF00069 | 0.711 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.621 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.788 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.502 |
MOD_GlcNHglycan | 48 | 52 | PF01048 | 0.463 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.609 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.712 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.744 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.627 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.402 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.749 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.830 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.618 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.634 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.649 |
MOD_PK_1 | 241 | 247 | PF00069 | 0.616 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.607 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.736 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.630 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.747 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.611 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.545 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.444 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.735 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.765 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.666 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.727 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.773 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.803 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.655 |
MOD_SUMO_for_1 | 310 | 313 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 331 | 336 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 123 | 128 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_4 | 136 | 142 | PF01217 | 0.521 |
TRG_DiLeu_BaEn_4 | 331 | 337 | PF01217 | 0.610 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.683 |
TRG_DiLeu_LyEn_5 | 123 | 128 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.674 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 125 | 129 | PF00026 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB32 | Leptomonas seymouri | 48% | 96% |
A0A3S5H577 | Leishmania donovani | 88% | 100% |
A4H3T2 | Leishmania braziliensis | 70% | 100% |
A4HS07 | Leishmania infantum | 88% | 100% |
Q9GRM8 | Leishmania major | 88% | 100% |