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: Q4Q814
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 211 | 213 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.485 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.559 |
DEG_SPOP_SBC_1 | 171 | 175 | PF00917 | 0.581 |
DEG_SPOP_SBC_1 | 256 | 260 | PF00917 | 0.619 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.608 |
DOC_CYCLIN_RxL_1 | 454 | 467 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 45 | 51 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 304 | 313 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 496 | 504 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 52 | 59 | PF00069 | 0.527 |
DOC_PP2B_PxIxI_1 | 445 | 451 | PF00149 | 0.427 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.614 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.472 |
LIG_14-3-3_CanoR_1 | 75 | 84 | PF00244 | 0.615 |
LIG_APCC_ABBA_1 | 57 | 62 | PF00400 | 0.539 |
LIG_BIR_III_2 | 340 | 344 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 30 | 34 | PF00533 | 0.523 |
LIG_CaM_IQ_9 | 474 | 490 | PF13499 | 0.379 |
LIG_deltaCOP1_diTrp_1 | 404 | 412 | PF00928 | 0.565 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.615 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.507 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.542 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.608 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.510 |
LIG_FXI_DFP_1 | 409 | 413 | PF00024 | 0.627 |
LIG_Integrin_isoDGR_2 | 296 | 298 | PF01839 | 0.495 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.560 |
LIG_PDZ_Class_1 | 506 | 511 | PF00595 | 0.528 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 309 | 313 | PF00017 | 0.549 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.539 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.476 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.556 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.703 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.593 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.607 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.472 |
LIG_SH3_CIN85_PxpxPR_1 | 47 | 52 | PF14604 | 0.476 |
LIG_SUMO_SIM_par_1 | 427 | 433 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 499 | 505 | PF11976 | 0.524 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.566 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.533 |
LIG_WW_3 | 49 | 53 | PF00397 | 0.596 |
MOD_CDK_SPK_2 | 224 | 229 | PF00069 | 0.616 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.612 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.769 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.646 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.396 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.607 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.571 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.642 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.498 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.465 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.468 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.535 |
MOD_Cter_Amidation | 73 | 76 | PF01082 | 0.629 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.573 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.581 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.622 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.627 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.731 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.575 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.688 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.631 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.671 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.643 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.410 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.649 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.607 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.729 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.665 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.666 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.598 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.593 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.532 |
MOD_NEK2_2 | 172 | 177 | PF00069 | 0.683 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.622 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.622 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.526 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.622 |
MOD_PKB_1 | 154 | 162 | PF00069 | 0.579 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.520 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.563 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.639 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.467 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.599 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.465 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.467 |
MOD_SUMO_rev_2 | 351 | 356 | PF00179 | 0.551 |
TRG_DiLeu_BaEn_1 | 190 | 195 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_2 | 450 | 456 | PF01217 | 0.384 |
TRG_DiLeu_BaEn_4 | 418 | 424 | PF01217 | 0.579 |
TRG_DiLeu_BaLyEn_6 | 189 | 194 | PF01217 | 0.577 |
TRG_DiLeu_BaLyEn_6 | 41 | 46 | PF01217 | 0.505 |
TRG_DiLeu_BaLyEn_6 | 458 | 463 | PF01217 | 0.369 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 20 | 22 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 495 | 498 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.739 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.548 |
TRG_NLS_Bipartite_1 | 196 | 214 | PF00514 | 0.527 |
TRG_NLS_MonoExtC_3 | 209 | 214 | PF00514 | 0.555 |
TRG_NLS_MonoExtN_4 | 209 | 214 | PF00514 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 316 | 320 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA28 | Leptomonas seymouri | 44% | 100% |
A0A3S5H7K0 | Leishmania donovani | 85% | 99% |
A4HGV1 | Leishmania braziliensis | 65% | 100% |
A4I3Y1 | Leishmania infantum | 85% | 99% |
E9B071 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |