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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B4T1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.643 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.634 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 298 | 306 | PF00400 | 0.614 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.631 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.654 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.485 |
DOC_ANK_TNKS_1 | 254 | 261 | PF00023 | 0.496 |
DOC_CKS1_1 | 328 | 333 | PF01111 | 0.567 |
DOC_CYCLIN_RxL_1 | 331 | 338 | PF00134 | 0.642 |
DOC_CYCLIN_RxL_1 | 37 | 46 | PF00134 | 0.659 |
DOC_MAPK_gen_1 | 298 | 304 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 314 | 322 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 39 | 45 | PF00069 | 0.584 |
DOC_MAPK_HePTP_8 | 316 | 328 | PF00069 | 0.700 |
DOC_MAPK_MEF2A_6 | 203 | 210 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.695 |
DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 78 | 85 | PF00069 | 0.705 |
DOC_PP2B_LxvP_1 | 74 | 77 | PF13499 | 0.486 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.730 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 314 | 322 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.580 |
LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.612 |
LIG_BRCT_BRCA1_1 | 382 | 386 | PF00533 | 0.593 |
LIG_CaM_NSCaTE_8 | 289 | 296 | PF13499 | 0.302 |
LIG_deltaCOP1_diTrp_1 | 5 | 11 | PF00928 | 0.581 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.705 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.545 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.475 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.594 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.604 |
LIG_GBD_Chelix_1 | 332 | 340 | PF00786 | 0.645 |
LIG_Integrin_RGD_1 | 284 | 286 | PF01839 | 0.398 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 375 | 380 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.547 |
LIG_MAD2 | 40 | 48 | PF02301 | 0.657 |
LIG_NRBOX | 167 | 173 | PF00104 | 0.597 |
LIG_PCNA_yPIPBox_3 | 366 | 380 | PF02747 | 0.644 |
LIG_Pex14_2 | 337 | 341 | PF04695 | 0.509 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.476 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.501 |
LIG_SH3_1 | 307 | 313 | PF00018 | 0.598 |
LIG_SH3_2 | 310 | 315 | PF14604 | 0.609 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.453 |
LIG_SH3_3 | 307 | 313 | PF00018 | 0.646 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.594 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.597 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.720 |
LIG_SUMO_SIM_par_1 | 41 | 46 | PF11976 | 0.649 |
LIG_TRAF2_1 | 271 | 274 | PF00917 | 0.704 |
MOD_CDK_SPK_2 | 52 | 57 | PF00069 | 0.490 |
MOD_CDK_SPxxK_3 | 248 | 255 | PF00069 | 0.584 |
MOD_CDK_SPxxK_3 | 327 | 334 | PF00069 | 0.645 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.706 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.675 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.654 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.569 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.601 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.695 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.662 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.640 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.736 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.660 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.615 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.511 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.603 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.664 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.602 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.721 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.720 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.503 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.606 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.587 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.740 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.527 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.662 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.508 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.429 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.675 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.663 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.709 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.741 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.787 |
MOD_LATS_1 | 120 | 126 | PF00433 | 0.674 |
MOD_LATS_1 | 138 | 144 | PF00433 | 0.486 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.712 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.661 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.613 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.597 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.504 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.501 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.662 |
MOD_NEK2_2 | 81 | 86 | PF00069 | 0.501 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.679 |
MOD_PK_1 | 122 | 128 | PF00069 | 0.669 |
MOD_PKA_1 | 236 | 242 | PF00069 | 0.679 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.699 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.689 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.734 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.455 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.679 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.600 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.793 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.603 |
MOD_Plk_2-3 | 224 | 230 | PF00069 | 0.593 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.573 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.641 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.526 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.599 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.568 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.734 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.749 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.535 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.708 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.574 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.685 |
MOD_SUMO_rev_2 | 88 | 96 | PF00179 | 0.784 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.655 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 38 | 40 | PF00400 | 0.664 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P9L5 | Trypanosomatidae | 25% | 94% |
A0A3Q8II07 | Leishmania donovani | 86% | 100% |
A4HAM8 | Leishmania braziliensis | 67% | 100% |
A4I9S0 | Leishmania infantum | 86% | 70% |
C9ZMW2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
Q4Q395 | Leishmania major | 87% | 99% |