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: A4HPC3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.698 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.739 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.443 |
DEG_APCC_DBOX_1 | 300 | 308 | PF00400 | 0.732 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.713 |
DOC_CKS1_1 | 34 | 39 | PF01111 | 0.487 |
DOC_MAPK_gen_1 | 126 | 134 | PF00069 | 0.695 |
DOC_MAPK_gen_1 | 40 | 49 | PF00069 | 0.638 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.707 |
DOC_PP1_RVXF_1 | 257 | 264 | PF00149 | 0.707 |
DOC_PP4_FxxP_1 | 146 | 149 | PF00568 | 0.707 |
DOC_PP4_FxxP_1 | 270 | 273 | PF00568 | 0.460 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.680 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 177 | 182 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.747 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.770 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.659 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.745 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.637 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.570 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.691 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.681 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.671 |
LIG_IRF3_LxIS_1 | 128 | 135 | PF10401 | 0.466 |
LIG_LIR_Apic_2 | 144 | 149 | PF02991 | 0.704 |
LIG_LIR_Gen_1 | 355 | 365 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 366 | 373 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 70 | 79 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 70 | 74 | PF02991 | 0.402 |
LIG_LYPXL_yS_3 | 52 | 55 | PF13949 | 0.683 |
LIG_PDZ_Class_3 | 368 | 373 | PF00595 | 0.753 |
LIG_SH2_CRK | 231 | 235 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 357 | 360 | PF00017 | 0.591 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.682 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 247 | 251 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.591 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.459 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.505 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.742 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.643 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.617 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.610 |
MOD_CDK_SPxxK_3 | 33 | 40 | PF00069 | 0.494 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.615 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.602 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.728 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.691 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.558 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.696 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.572 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.718 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.608 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.663 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.657 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.750 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.599 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.533 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.703 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.448 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.714 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.574 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.586 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.568 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.599 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.681 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.662 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.742 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.677 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.623 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.607 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.708 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.550 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.382 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.517 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.625 |
MOD_PIKK_1 | 224 | 230 | PF00454 | 0.719 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.476 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.661 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.574 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.617 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.591 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.590 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.657 |
MOD_PKB_1 | 175 | 183 | PF00069 | 0.456 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.611 |
MOD_Plk_1 | 191 | 197 | PF00069 | 0.653 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.713 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.512 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.579 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.733 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.680 |
MOD_Plk_2-3 | 165 | 171 | PF00069 | 0.708 |
MOD_Plk_2-3 | 183 | 189 | PF00069 | 0.649 |
MOD_Plk_2-3 | 70 | 76 | PF00069 | 0.695 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.658 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.674 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.672 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.635 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.743 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.640 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.549 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.622 |
TRG_DiLeu_BaEn_4 | 302 | 308 | PF01217 | 0.584 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.599 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.683 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 257 | 259 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.602 |
TRG_ER_diArg_1 | 347 | 349 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 42 | 44 | PF00400 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.612 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYX6 | Leptomonas seymouri | 60% | 97% |
A0A1X0P7K9 | Trypanosomatidae | 38% | 100% |
A0A3Q8IKB1 | Leishmania donovani | 81% | 100% |
A0A3R7K7R7 | Trypanosoma rangeli | 41% | 100% |
A4ICG1 | Leishmania infantum | 80% | 100% |
D0A3D6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AT32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q1G6 | Leishmania major | 81% | 100% |
V5BH32 | Trypanosoma cruzi | 37% | 100% |