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: A0A3S7WWD4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.598 |
CLV_C14_Caspase3-7 | 72 | 76 | PF00656 | 0.603 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.595 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 370 | 372 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.681 |
DEG_SCF_TRCP1_1 | 75 | 80 | PF00400 | 0.647 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.675 |
DOC_CKS1_1 | 71 | 76 | PF01111 | 0.588 |
DOC_MAPK_gen_1 | 262 | 271 | PF00069 | 0.702 |
DOC_MAPK_gen_1 | 303 | 312 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 310 | 313 | PF13499 | 0.678 |
DOC_PP2B_LxvP_1 | 87 | 90 | PF13499 | 0.546 |
DOC_PP2B_PxIxI_1 | 89 | 95 | PF00149 | 0.542 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.648 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 225 | 230 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 262 | 271 | PF00244 | 0.702 |
LIG_14-3-3_CanoR_1 | 303 | 313 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 356 | 363 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 4 | 12 | PF00244 | 0.635 |
LIG_APCC_ABBA_1 | 337 | 342 | PF00400 | 0.581 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.667 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.642 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.484 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.789 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.567 |
LIG_FHA_1 | 305 | 311 | PF00498 | 0.749 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.531 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.599 |
LIG_LIR_Apic_2 | 65 | 70 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.716 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.559 |
LIG_LYPXL_yS_3 | 249 | 252 | PF13949 | 0.573 |
LIG_NRP_CendR_1 | 385 | 388 | PF00754 | 0.704 |
LIG_PCNA_yPIPBox_3 | 156 | 167 | PF02747 | 0.657 |
LIG_PTB_Apo_2 | 52 | 59 | PF02174 | 0.643 |
LIG_PTB_Phospho_1 | 52 | 58 | PF10480 | 0.647 |
LIG_SH2_NCK_1 | 15 | 19 | PF00017 | 0.651 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.700 |
LIG_SH3_1 | 202 | 208 | PF00018 | 0.619 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.739 |
LIG_SH3_3 | 179 | 185 | PF00018 | 0.674 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.542 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.539 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.595 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.632 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.692 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.631 |
LIG_SUMO_SIM_par_1 | 242 | 247 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 90 | 95 | PF11976 | 0.541 |
LIG_TRAF2_1 | 283 | 286 | PF00917 | 0.602 |
LIG_TYR_ITSM | 245 | 252 | PF00017 | 0.574 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.581 |
MOD_CDK_SPK_2 | 99 | 104 | PF00069 | 0.575 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.733 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.660 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.521 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.534 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.636 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.679 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.571 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.678 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.812 |
MOD_Cter_Amidation | 383 | 386 | PF01082 | 0.599 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.679 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.665 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.730 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.705 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.781 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.517 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.451 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.760 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.587 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.673 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.780 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.604 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.438 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.488 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.572 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.699 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.649 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.683 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.727 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.565 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.584 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.578 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.619 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.745 |
MOD_NEK2_2 | 113 | 118 | PF00069 | 0.588 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.582 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.707 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.759 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.521 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.706 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.620 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.679 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.711 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.527 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.579 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.679 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.599 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.544 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.587 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.718 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.627 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 385 | 388 | PF00400 | 0.715 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8I5 | Leptomonas seymouri | 39% | 81% |
A4HBQ6 | Leishmania braziliensis | 65% | 98% |
A4HZ58 | Leishmania infantum | 100% | 100% |
E9AV26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 99% |
Q4QCF6 | Leishmania major | 88% | 100% |