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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4Q641
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.785 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.788 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.479 |
CLV_PCSK_PC7_1 | 40 | 46 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.574 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.592 |
DEG_COP1_1 | 433 | 443 | PF00400 | 0.620 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.615 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 77 | 83 | PF00134 | 0.510 |
DOC_MAPK_gen_1 | 343 | 350 | PF00069 | 0.651 |
DOC_MAPK_MEF2A_6 | 68 | 77 | PF00069 | 0.533 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.529 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.568 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.748 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 214 | 218 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 221 | 227 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 299 | 304 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.542 |
LIG_BRCT_BRCA1_1 | 270 | 274 | PF00533 | 0.645 |
LIG_BRCT_BRCA1_1 | 420 | 424 | PF00533 | 0.656 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.473 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.598 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.739 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.705 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.593 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.644 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.707 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 125 | 130 | PF02991 | 0.636 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 442 | 452 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.747 |
LIG_PDZ_Class_2 | 480 | 485 | PF00595 | 0.539 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.607 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.597 |
LIG_SH2_NCK_1 | 137 | 141 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.528 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.754 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.630 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.749 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.683 |
LIG_TRAF2_1 | 195 | 198 | PF00917 | 0.559 |
LIG_TRAF2_1 | 354 | 357 | PF00917 | 0.547 |
LIG_TRFH_1 | 137 | 141 | PF08558 | 0.614 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.626 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.717 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.667 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.640 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.685 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.614 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.658 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.630 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.666 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.444 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.643 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.633 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.700 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.582 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.595 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.551 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.672 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.682 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.610 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.700 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.647 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.692 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.647 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.649 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.693 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.637 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.585 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.641 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.578 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.631 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.627 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.667 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.585 |
MOD_N-GLC_2 | 98 | 100 | PF02516 | 0.664 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.765 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.727 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.663 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.489 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.613 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.680 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.584 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.710 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.677 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.532 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.794 |
MOD_PKA_1 | 299 | 305 | PF00069 | 0.704 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.640 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.643 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.765 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.671 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.651 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.704 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.685 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.590 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.662 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.654 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.689 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.638 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.657 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.637 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.559 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.553 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.691 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.551 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.566 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.612 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.634 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.748 |
MOD_SUMO_rev_2 | 186 | 194 | PF00179 | 0.666 |
MOD_SUMO_rev_2 | 452 | 456 | PF00179 | 0.563 |
TRG_DiLeu_BaEn_4 | 453 | 459 | PF01217 | 0.564 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 96 | 99 | PF00400 | 0.528 |
TRG_NES_CRM1_1 | 65 | 79 | PF08389 | 0.628 |
TRG_NLS_MonoExtC_3 | 469 | 474 | PF00514 | 0.494 |
TRG_NLS_MonoExtN_4 | 468 | 474 | PF00514 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4Q7 | Leishmania donovani | 82% | 100% |
A4HJK2 | Leishmania braziliensis | 54% | 100% |
A4I703 | Leishmania infantum | 83% | 100% |
E9B221 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |