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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QJ84
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.797 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.575 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.793 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 171 | 177 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 422 | 428 | PF00082 | 0.803 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.516 |
DEG_MDM2_SWIB_1 | 161 | 168 | PF02201 | 0.573 |
DEG_SCF_FBW7_2 | 384 | 390 | PF00400 | 0.594 |
DOC_CKS1_1 | 356 | 361 | PF01111 | 0.701 |
DOC_CKS1_1 | 384 | 389 | PF01111 | 0.595 |
DOC_CYCLIN_RxL_1 | 403 | 414 | PF00134 | 0.585 |
DOC_CYCLIN_yCln2_LP_2 | 84 | 90 | PF00134 | 0.581 |
DOC_MAPK_gen_1 | 36 | 45 | PF00069 | 0.634 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.516 |
DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.610 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.681 |
DOC_USP7_MATH_2 | 281 | 287 | PF00917 | 0.665 |
DOC_USP7_UBL2_3 | 180 | 184 | PF12436 | 0.578 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 117 | 123 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 143 | 152 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.592 |
LIG_BIR_III_2 | 379 | 383 | PF00653 | 0.628 |
LIG_BIR_III_4 | 109 | 113 | PF00653 | 0.550 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.683 |
LIG_CtBP_PxDLS_1 | 282 | 288 | PF00389 | 0.738 |
LIG_deltaCOP1_diTrp_1 | 195 | 202 | PF00928 | 0.450 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.610 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.641 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.560 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.585 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.592 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.609 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.591 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.599 |
LIG_Integrin_RGD_1 | 207 | 209 | PF01839 | 0.507 |
LIG_Integrin_RGD_1 | 302 | 304 | PF01839 | 0.615 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 252 | 263 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 327 | 333 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 121 | 125 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.644 |
LIG_LRP6_Inhibitor_1 | 137 | 143 | PF00058 | 0.548 |
LIG_Pex14_1 | 134 | 138 | PF04695 | 0.504 |
LIG_Pex14_1 | 296 | 300 | PF04695 | 0.599 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.444 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.566 |
LIG_SH2_GRB2like | 138 | 141 | PF00017 | 0.504 |
LIG_SH2_STAT3 | 222 | 225 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 333 | 336 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.648 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.679 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.649 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.658 |
LIG_TRAF2_1 | 214 | 217 | PF00917 | 0.495 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.607 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.658 |
LIG_TRAF2_1 | 62 | 65 | PF00917 | 0.624 |
LIG_UBA3_1 | 14 | 19 | PF00899 | 0.617 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.615 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.690 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.499 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.595 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.602 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.569 |
MOD_CMANNOS | 199 | 202 | PF00535 | 0.455 |
MOD_GlcNHglycan | 283 | 288 | PF01048 | 0.694 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.669 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.721 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.579 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.697 |
MOD_N-GLC_1 | 10 | 15 | PF02516 | 0.576 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.685 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.554 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.437 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.559 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.526 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.573 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.655 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.597 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.772 |
MOD_PKA_1 | 179 | 185 | PF00069 | 0.598 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.682 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.642 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.567 |
MOD_PKB_1 | 391 | 399 | PF00069 | 0.651 |
MOD_Plk_1 | 10 | 16 | PF00069 | 0.590 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.485 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.687 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.597 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.696 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.599 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.499 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.602 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.704 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.599 |
MOD_SUMO_for_1 | 68 | 71 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 276 | 281 | PF00179 | 0.680 |
MOD_SUMO_rev_2 | 64 | 68 | PF00179 | 0.506 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.559 |
TRG_ER_diArg_1 | 175 | 177 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.676 |
TRG_ER_diArg_1 | 391 | 394 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYF1 | Leptomonas seymouri | 90% | 92% |
A0A0S4IU67 | Bodo saltans | 63% | 100% |
A0A1X0NK32 | Trypanosomatidae | 74% | 93% |
A0A3S7WP90 | Leishmania donovani | 100% | 100% |
A4H4G2 | Leishmania braziliensis | 96% | 88% |
A4HSN9 | Leishmania infantum | 100% | 100% |
C9ZNE2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 93% |
E9AKM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
V5BGD5 | Trypanosoma cruzi | 76% | 100% |