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: A0A3Q8IQI6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.550 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.643 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 462 | 464 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.609 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.413 |
DEG_COP1_1 | 187 | 197 | PF00400 | 0.650 |
DEG_SCF_SKP2-CKS1_1 | 454 | 461 | PF00560 | 0.567 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.661 |
DOC_CYCLIN_yCln2_LP_2 | 134 | 140 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 16 | 24 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 329 | 335 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 16 | 24 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.573 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.621 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.573 |
DOC_USP7_UBL2_3 | 361 | 365 | PF12436 | 0.460 |
DOC_USP7_UBL2_3 | 388 | 392 | PF12436 | 0.649 |
DOC_USP7_UBL2_3 | 407 | 411 | PF12436 | 0.424 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 186 | 194 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 19 | 25 | PF00244 | 0.409 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.563 |
LIG_BIR_III_4 | 363 | 367 | PF00653 | 0.466 |
LIG_BRCT_BRCA1_1 | 355 | 359 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_2 | 355 | 361 | PF00533 | 0.524 |
LIG_CSL_BTD_1 | 58 | 61 | PF09270 | 0.400 |
LIG_CtBP_PxDLS_1 | 157 | 161 | PF00389 | 0.515 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.559 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.512 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.421 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.394 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.491 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.584 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.552 |
LIG_HCF-1_HBM_1 | 28 | 31 | PF13415 | 0.415 |
LIG_Integrin_isoDGR_2 | 222 | 224 | PF01839 | 0.595 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.459 |
LIG_PCNA_yPIPBox_3 | 329 | 339 | PF02747 | 0.420 |
LIG_PTB_Apo_2 | 69 | 76 | PF02174 | 0.479 |
LIG_SH2_STAT3 | 65 | 68 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.416 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.455 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.552 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.497 |
LIG_SH3_4 | 361 | 368 | PF00018 | 0.441 |
LIG_SUMO_SIM_anti_2 | 53 | 59 | PF11976 | 0.373 |
LIG_SUMO_SIM_par_1 | 126 | 131 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.401 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.592 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 455 | 462 | PF00069 | 0.605 |
MOD_CDK_SPxxK_3 | 78 | 85 | PF00069 | 0.620 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.685 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.700 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.784 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.594 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.624 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.596 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.495 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.619 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.574 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.622 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.680 |
MOD_CK2_1 | 288 | 294 | PF00069 | 0.670 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.415 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.634 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.637 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.521 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.569 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.746 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.580 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.642 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.578 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.507 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.460 |
MOD_GlcNHglycan | 439 | 443 | PF01048 | 0.779 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.560 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.586 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.676 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.587 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.666 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.566 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.602 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.730 |
MOD_N-GLC_1 | 234 | 239 | PF02516 | 0.632 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.622 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.544 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.551 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.556 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.556 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.603 |
MOD_NEK2_2 | 163 | 168 | PF00069 | 0.385 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.560 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.690 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.644 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.459 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.564 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.630 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.470 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.483 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.606 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.640 |
MOD_Plk_2-3 | 425 | 431 | PF00069 | 0.641 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.477 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.572 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.700 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.670 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.622 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.618 |
MOD_SUMO_rev_2 | 208 | 218 | PF00179 | 0.647 |
MOD_SUMO_rev_2 | 313 | 323 | PF00179 | 0.517 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.666 |
TRG_NLS_Bipartite_1 | 397 | 411 | PF00514 | 0.447 |
TRG_NLS_MonoCore_2 | 460 | 465 | PF00514 | 0.633 |
TRG_NLS_MonoExtC_3 | 406 | 411 | PF00514 | 0.478 |
TRG_NLS_MonoExtC_3 | 460 | 465 | PF00514 | 0.633 |
TRG_NLS_MonoExtN_4 | 406 | 411 | PF00514 | 0.478 |
TRG_NLS_MonoExtN_4 | 459 | 466 | PF00514 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 243 | 247 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J3 | Leptomonas seymouri | 55% | 97% |
A4HGG9 | Leishmania braziliensis | 72% | 100% |
A4I3K1 | Leishmania infantum | 100% | 100% |
E9AZU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q8E4 | Leishmania major | 87% | 100% |