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: E9B5A7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.619 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.692 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.647 |
CLV_PCSK_PC7_1 | 313 | 319 | PF00082 | 0.602 |
CLV_PCSK_PC7_1 | 331 | 337 | PF00082 | 0.634 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.628 |
DEG_COP1_1 | 160 | 167 | PF00400 | 0.518 |
DOC_ANK_TNKS_1 | 338 | 345 | PF00023 | 0.620 |
DOC_CKS1_1 | 135 | 140 | PF01111 | 0.528 |
DOC_MAPK_gen_1 | 258 | 267 | PF00069 | 0.655 |
DOC_MAPK_gen_1 | 70 | 79 | PF00069 | 0.621 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.625 |
DOC_USP7_MATH_2 | 158 | 164 | PF00917 | 0.603 |
DOC_USP7_MATH_2 | 391 | 397 | PF00917 | 0.496 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 140 | 145 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 108 | 116 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 184 | 189 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 277 | 285 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 313 | 317 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 55 | 62 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 87 | 95 | PF00244 | 0.649 |
LIG_BIR_III_2 | 371 | 375 | PF00653 | 0.481 |
LIG_Clathr_ClatBox_1 | 241 | 245 | PF01394 | 0.538 |
LIG_deltaCOP1_diTrp_1 | 15 | 22 | PF00928 | 0.453 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.606 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.567 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.405 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.566 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.548 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.575 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.573 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.637 |
LIG_PALB2_WD40_1 | 5 | 13 | PF16756 | 0.449 |
LIG_PTAP_UEV_1 | 202 | 207 | PF05743 | 0.654 |
LIG_SH2_STAP1 | 14 | 18 | PF00017 | 0.514 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.619 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.641 |
LIG_SUMO_SIM_anti_2 | 262 | 272 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 160 | 166 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 262 | 272 | PF11976 | 0.473 |
LIG_SUMO_SIM_par_1 | 34 | 40 | PF11976 | 0.407 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.686 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.441 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.626 |
LIG_TRAF2_1 | 391 | 394 | PF00917 | 0.593 |
LIG_TRAF2_1 | 89 | 92 | PF00917 | 0.548 |
MOD_CDC14_SPxK_1 | 207 | 210 | PF00782 | 0.533 |
MOD_CDK_SPxK_1 | 204 | 210 | PF00069 | 0.527 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.669 |
MOD_CDK_SPxxK_3 | 305 | 312 | PF00069 | 0.623 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.692 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.669 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.562 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.768 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.556 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.622 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.407 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.783 |
MOD_Cter_Amidation | 343 | 346 | PF01082 | 0.625 |
MOD_Cter_Amidation | 85 | 88 | PF01082 | 0.506 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.710 |
MOD_GlcNHglycan | 15 | 19 | PF01048 | 0.578 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.657 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.526 |
MOD_GlcNHglycan | 270 | 276 | PF01048 | 0.560 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.588 |
MOD_GlcNHglycan | 295 | 299 | PF01048 | 0.601 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.699 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.686 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.732 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.555 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.649 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.572 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.636 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.613 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.581 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.750 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.566 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.515 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.756 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.536 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.607 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.676 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.495 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.574 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.627 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.486 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.631 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.553 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.640 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.697 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.672 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.620 |
MOD_PKA_1 | 312 | 318 | PF00069 | 0.633 |
MOD_PKA_1 | 345 | 351 | PF00069 | 0.698 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.648 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.755 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.723 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.668 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.656 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.528 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.698 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.500 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.546 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.522 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.618 |
MOD_PKB_1 | 61 | 69 | PF00069 | 0.530 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.636 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.624 |
MOD_Plk_4 | 209 | 215 | PF00069 | 0.605 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.655 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.717 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.654 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.729 |
MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.719 |
TRG_DiLeu_BaEn_1 | 260 | 265 | PF01217 | 0.458 |
TRG_DiLeu_BaEn_1 | 91 | 96 | PF01217 | 0.546 |
TRG_ER_diArg_1 | 335 | 337 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.706 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB80 | Leptomonas seymouri | 34% | 74% |
A0A3Q8IFR9 | Leishmania donovani | 81% | 100% |
A4HB37 | Leishmania braziliensis | 56% | 99% |
A4IAN2 | Leishmania infantum | 82% | 100% |
Q4Q2M6 | Leishmania major | 85% | 100% |