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: A0A3Q8IFR9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.688 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.639 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 311 | 313 | PF00082 | 0.738 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.690 |
CLV_PCSK_PC7_1 | 312 | 318 | PF00082 | 0.632 |
CLV_PCSK_PC7_1 | 330 | 336 | PF00082 | 0.692 |
CLV_PCSK_PC7_1 | 379 | 385 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.693 |
DOC_ANK_TNKS_1 | 337 | 344 | PF00023 | 0.689 |
DOC_MAPK_gen_1 | 258 | 267 | PF00069 | 0.678 |
DOC_MAPK_gen_1 | 69 | 79 | PF00069 | 0.656 |
DOC_PP4_FxxP_1 | 10 | 13 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.697 |
DOC_USP7_MATH_2 | 158 | 164 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 276 | 284 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.761 |
LIG_Actin_WH2_2 | 31 | 49 | PF00022 | 0.459 |
LIG_BIR_III_2 | 198 | 202 | PF00653 | 0.637 |
LIG_Clathr_ClatBox_1 | 241 | 245 | PF01394 | 0.573 |
LIG_deltaCOP1_diTrp_1 | 15 | 22 | PF00928 | 0.492 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.597 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.580 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.648 |
LIG_FHA_2 | 289 | 295 | PF00498 | 0.677 |
LIG_FHA_2 | 376 | 382 | PF00498 | 0.617 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.683 |
LIG_LIR_Gen_1 | 15 | 23 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 262 | 272 | PF02991 | 0.602 |
LIG_LIR_Nem_3 | 15 | 19 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 262 | 267 | PF02991 | 0.549 |
LIG_PTAP_UEV_1 | 202 | 207 | PF05743 | 0.712 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.593 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.662 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.656 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.746 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.599 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.629 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.721 |
MOD_CDK_SPxxK_3 | 304 | 311 | PF00069 | 0.695 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.698 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.685 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.587 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.630 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.587 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.613 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.567 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.733 |
MOD_Cter_Amidation | 324 | 327 | PF01082 | 0.621 |
MOD_Cter_Amidation | 342 | 345 | PF01082 | 0.706 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.733 |
MOD_GlcNHglycan | 15 | 19 | PF01048 | 0.600 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.707 |
MOD_GlcNHglycan | 269 | 275 | PF01048 | 0.613 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.656 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.657 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.732 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.667 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.632 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.612 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.744 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.597 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.690 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.521 |
MOD_LATS_1 | 182 | 188 | PF00433 | 0.616 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.566 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.768 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.612 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.606 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.640 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.664 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.644 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.630 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.662 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.733 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.759 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.667 |
MOD_PKA_1 | 311 | 317 | PF00069 | 0.654 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.615 |
MOD_PKA_1 | 344 | 350 | PF00069 | 0.734 |
MOD_PKA_1 | 384 | 390 | PF00069 | 0.606 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.534 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.692 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.607 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.744 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.692 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.740 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.633 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.661 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.734 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.637 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.767 |
MOD_PKB_1 | 324 | 332 | PF00069 | 0.604 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.476 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.627 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.567 |
MOD_Plk_4 | 134 | 140 | PF00069 | 0.671 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.694 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.691 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.611 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.640 |
MOD_ProDKin_1 | 140 | 146 | PF00069 | 0.711 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.650 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.765 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.565 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.554 |
MOD_SUMO_rev_2 | 230 | 237 | PF00179 | 0.550 |
TRG_DiLeu_BaEn_2 | 259 | 265 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.560 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.596 |
TRG_NLS_MonoExtC_3 | 315 | 321 | PF00514 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.496 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB80 | Leptomonas seymouri | 35% | 74% |
A4HB37 | Leishmania braziliensis | 55% | 99% |
A4IAN2 | Leishmania infantum | 99% | 100% |
E9B5A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q2M6 | Leishmania major | 85% | 100% |