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 | yes | yes: 5, no: 1 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9APS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.508 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.807 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.781 |
CLV_PCSK_FUR_1 | 121 | 125 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.752 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.807 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 358 | 360 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.760 |
CLV_Separin_Metazoa | 217 | 221 | PF03568 | 0.533 |
DEG_APCC_DBOX_1 | 219 | 227 | PF00400 | 0.606 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.581 |
DEG_SPOP_SBC_1 | 3 | 7 | PF00917 | 0.620 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 14 | 24 | PF00069 | 0.638 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 17 | 26 | PF00069 | 0.477 |
DOC_MAPK_RevD_3 | 167 | 181 | PF00069 | 0.518 |
DOC_MAPK_RevD_3 | 316 | 331 | PF00069 | 0.414 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.655 |
DOC_PP2B_PxIxI_1 | 315 | 321 | PF00149 | 0.566 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.513 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.413 |
LIG_14-3-3_CanoR_1 | 164 | 170 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 181 | 191 | PF00244 | 0.565 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.549 |
LIG_BIR_III_2 | 215 | 219 | PF00653 | 0.415 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.588 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.493 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.562 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.646 |
LIG_GBD_Chelix_1 | 29 | 37 | PF00786 | 0.550 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.492 |
LIG_PDZ_Class_2 | 421 | 426 | PF00595 | 0.411 |
LIG_Pex14_2 | 422 | 426 | PF04695 | 0.389 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.423 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.482 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.535 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.527 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 316 | 322 | PF11976 | 0.565 |
LIG_TRAF2_1 | 131 | 134 | PF00917 | 0.596 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.509 |
LIG_WW_3 | 217 | 221 | PF00397 | 0.693 |
MOD_CDC14_SPxK_1 | 141 | 144 | PF00782 | 0.534 |
MOD_CDK_SPxK_1 | 138 | 144 | PF00069 | 0.541 |
MOD_CDK_SPxxK_3 | 251 | 258 | PF00069 | 0.628 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.707 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.789 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.512 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.691 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.577 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.751 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.518 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.679 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.714 |
MOD_Cter_Amidation | 113 | 116 | PF01082 | 0.738 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.551 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.766 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.688 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.689 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.714 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.783 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.719 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.609 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.520 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.549 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.620 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.809 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.715 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.716 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.349 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.763 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.416 |
MOD_NEK2_2 | 165 | 170 | PF00069 | 0.672 |
MOD_NEK2_2 | 222 | 227 | PF00069 | 0.644 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.513 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.521 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.726 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.720 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.734 |
MOD_PKB_1 | 265 | 273 | PF00069 | 0.697 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.763 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.424 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.818 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.571 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.688 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.506 |
MOD_SUMO_rev_2 | 107 | 117 | PF00179 | 0.793 |
MOD_SUMO_rev_2 | 341 | 347 | PF00179 | 0.695 |
MOD_SUMO_rev_2 | 366 | 372 | PF00179 | 0.660 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.674 |
TRG_ER_diArg_1 | 178 | 181 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 264 | 267 | PF00400 | 0.703 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.639 |
TRG_NLS_Bipartite_1 | 179 | 200 | PF00514 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I683 | Leptomonas seymouri | 31% | 100% |
A0A3S7WT04 | Leishmania donovani | 81% | 100% |
A4H7N2 | Leishmania braziliensis | 53% | 94% |
A4HW21 | Leishmania infantum | 80% | 100% |
Q4QFQ6 | Leishmania major | 80% | 100% |