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: A4I6Z0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.608 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.667 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.671 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.640 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.587 |
DOC_CYCLIN_RxL_1 | 129 | 137 | PF00134 | 0.654 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.584 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.815 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 258 | 265 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 300 | 307 | PF00244 | 0.739 |
LIG_BIR_III_4 | 163 | 167 | PF00653 | 0.611 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.502 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.723 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.635 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.557 |
LIG_LIR_Apic_2 | 216 | 222 | PF02991 | 0.708 |
LIG_LIR_Apic_2 | 60 | 66 | PF02991 | 0.723 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.592 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.692 |
LIG_SH2_SRC | 188 | 191 | PF00017 | 0.691 |
LIG_SH2_STAT3 | 15 | 18 | PF00017 | 0.639 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.694 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.696 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.771 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.664 |
LIG_SUMO_SIM_par_1 | 80 | 88 | PF11976 | 0.576 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.728 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.821 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.728 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.699 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.546 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.646 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.681 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.593 |
MOD_Cter_Amidation | 354 | 357 | PF01082 | 0.711 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.714 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.519 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.649 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.610 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.574 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.621 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.712 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.678 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.804 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.674 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.682 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.787 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.673 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.558 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.643 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.612 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.686 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.640 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.692 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.810 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.648 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.667 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.636 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.569 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.546 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.723 |
MOD_N-GLC_1 | 301 | 306 | PF02516 | 0.654 |
MOD_N-GLC_2 | 328 | 330 | PF02516 | 0.631 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.729 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.670 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.692 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.628 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.652 |
MOD_PKA_1 | 258 | 264 | PF00069 | 0.670 |
MOD_PKA_1 | 267 | 273 | PF00069 | 0.609 |
MOD_PKA_1 | 320 | 326 | PF00069 | 0.637 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.607 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.709 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.738 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.698 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.643 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.597 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.612 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.584 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.585 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.747 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.534 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.817 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.797 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.705 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.638 |
MOD_SUMO_rev_2 | 232 | 237 | PF00179 | 0.649 |
MOD_SUMO_rev_2 | 260 | 270 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_1 | 33 | 38 | PF01217 | 0.528 |
TRG_ER_diLys_1 | 354 | 359 | PF00400 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 132 | 137 | PF00026 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 289 | 293 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILC0 | Leptomonas seymouri | 33% | 86% |
A0A3S5H7Q3 | Leishmania donovani | 100% | 100% |
A4HJJ2 | Leishmania braziliensis | 54% | 100% |
E9AEF6 | Leishmania major | 90% | 100% |
E9B211 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 96% |