Uncharacterized Protein, Uncharacterized
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4I403
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 429 | 433 | PF00656 | 0.734 |
CLV_NRD_NRD_1 | 144 | 146 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.846 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.760 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.713 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.730 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.848 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.713 |
CLV_PCSK_PC7_1 | 455 | 461 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.769 |
DEG_APCC_DBOX_1 | 14 | 22 | PF00400 | 0.693 |
DEG_APCC_DBOX_1 | 192 | 200 | PF00400 | 0.847 |
DEG_APCC_DBOX_1 | 423 | 431 | PF00400 | 0.739 |
DEG_SCF_FBW7_2 | 163 | 169 | PF00400 | 0.772 |
DEG_SPOP_SBC_1 | 205 | 209 | PF00917 | 0.771 |
DEG_SPOP_SBC_1 | 298 | 302 | PF00917 | 0.733 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.830 |
DOC_ANK_TNKS_1 | 289 | 296 | PF00023 | 0.818 |
DOC_CKS1_1 | 163 | 168 | PF01111 | 0.773 |
DOC_CKS1_1 | 175 | 180 | PF01111 | 0.591 |
DOC_CYCLIN_yCln2_LP_2 | 176 | 182 | PF00134 | 0.627 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.629 |
DOC_PP2B_LxvP_1 | 225 | 228 | PF13499 | 0.738 |
DOC_PP2B_LxvP_1 | 402 | 405 | PF13499 | 0.710 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.787 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.775 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.739 |
DOC_USP7_UBL2_3 | 121 | 125 | PF12436 | 0.745 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.806 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.750 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.843 |
LIG_14-3-3_CanoR_1 | 206 | 212 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 262 | 270 | PF00244 | 0.780 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.750 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 84 | 88 | PF00244 | 0.610 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.779 |
LIG_deltaCOP1_diTrp_1 | 413 | 416 | PF00928 | 0.702 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.669 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.776 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.654 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.658 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.737 |
LIG_GBD_Chelix_1 | 95 | 103 | PF00786 | 0.649 |
LIG_LIR_Apic_2 | 378 | 383 | PF02991 | 0.784 |
LIG_LIR_Gen_1 | 221 | 229 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 241 | 249 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.609 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.650 |
LIG_SH2_NCK_1 | 243 | 247 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.650 |
LIG_SH2_STAT3 | 439 | 442 | PF00017 | 0.704 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.776 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.756 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.539 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.680 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.840 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.736 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.659 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.679 |
LIG_SUMO_SIM_par_1 | 99 | 106 | PF11976 | 0.679 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.710 |
MOD_CDC14_SPxK_1 | 421 | 424 | PF00782 | 0.749 |
MOD_CDK_SPK_2 | 162 | 167 | PF00069 | 0.777 |
MOD_CDK_SPK_2 | 418 | 423 | PF00069 | 0.758 |
MOD_CDK_SPxK_1 | 418 | 424 | PF00069 | 0.758 |
MOD_CDK_SPxxK_3 | 114 | 121 | PF00069 | 0.691 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.637 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.775 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.659 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.802 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.601 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.555 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.741 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.601 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.869 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.636 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.665 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.624 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.764 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.581 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.741 |
MOD_CMANNOS | 411 | 414 | PF00535 | 0.756 |
MOD_Cter_Amidation | 294 | 297 | PF01082 | 0.783 |
MOD_DYRK1A_RPxSP_1 | 174 | 178 | PF00069 | 0.730 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.750 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.808 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.841 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.569 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.793 |
MOD_GlcNHglycan | 317 | 321 | PF01048 | 0.792 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.685 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.803 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.637 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.754 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.809 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.624 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.695 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.562 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.835 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.699 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.659 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.801 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.711 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.645 |
MOD_N-GLC_1 | 326 | 331 | PF02516 | 0.765 |
MOD_N-GLC_2 | 438 | 440 | PF02516 | 0.557 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.648 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.766 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.711 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.578 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.678 |
MOD_NEK2_2 | 238 | 243 | PF00069 | 0.631 |
MOD_NEK2_2 | 304 | 309 | PF00069 | 0.741 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.571 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.778 |
MOD_PIKK_1 | 278 | 284 | PF00454 | 0.812 |
MOD_PIKK_1 | 336 | 342 | PF00454 | 0.746 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.711 |
MOD_PKA_1 | 144 | 150 | PF00069 | 0.751 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.770 |
MOD_PKA_1 | 262 | 268 | PF00069 | 0.782 |
MOD_PKA_1 | 296 | 302 | PF00069 | 0.777 |
MOD_PKA_1 | 336 | 342 | PF00069 | 0.649 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.751 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.625 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.848 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.605 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.654 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.649 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.802 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.731 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.627 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.758 |
MOD_PKB_1 | 309 | 317 | PF00069 | 0.861 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.596 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.540 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.530 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.681 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.611 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.713 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.598 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.805 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.758 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.819 |
TRG_ER_diArg_1 | 144 | 146 | PF00400 | 0.786 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.775 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.865 |
TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.733 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IID2 | Leishmania donovani | 100% | 100% |
A4HGX3 | Leishmania braziliensis | 59% | 93% |
E9B093 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q7Z2 | Leishmania major | 92% | 100% |