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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4I7P9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.724 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.787 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.563 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.489 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.541 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.612 |
DEG_ODPH_VHL_1 | 173 | 185 | PF01847 | 0.509 |
DEG_SCF_FBW7_1 | 343 | 350 | PF00400 | 0.725 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 367 | 371 | PF00917 | 0.759 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.733 |
DOC_CKS1_1 | 457 | 462 | PF01111 | 0.665 |
DOC_MAPK_gen_1 | 114 | 121 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 177 | 185 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 187 | 197 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 114 | 121 | PF00069 | 0.490 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.599 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.522 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 289 | 292 | PF00568 | 0.676 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.674 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.605 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.557 |
DOC_USP7_MATH_2 | 314 | 320 | PF00917 | 0.765 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 114 | 120 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 15 | 22 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 451 | 460 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 67 | 75 | PF00244 | 0.566 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.708 |
LIG_deltaCOP1_diTrp_1 | 50 | 57 | PF00928 | 0.425 |
LIG_EH_1 | 286 | 290 | PF12763 | 0.662 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.527 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.621 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.473 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.774 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.784 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.839 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.607 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.650 |
LIG_LIR_Apic_2 | 150 | 155 | PF02991 | 0.528 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.660 |
LIG_LIR_Apic_2 | 455 | 460 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 46 | 53 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 447 | 453 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.543 |
LIG_LYPXL_yS_3 | 58 | 61 | PF13949 | 0.644 |
LIG_NBox_RRM_1 | 318 | 328 | PF00076 | 0.757 |
LIG_Pex14_2 | 285 | 289 | PF04695 | 0.692 |
LIG_Pex14_2 | 450 | 454 | PF04695 | 0.633 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.631 |
LIG_PTB_Apo_2 | 279 | 286 | PF02174 | 0.655 |
LIG_SH2_STAP1 | 368 | 372 | PF00017 | 0.804 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.530 |
LIG_SH3_2 | 109 | 114 | PF14604 | 0.542 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.545 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.479 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.689 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.672 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.817 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.647 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.583 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.525 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.734 |
LIG_WW_1 | 79 | 82 | PF00397 | 0.523 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.763 |
MOD_CDK_SPxK_1 | 18 | 24 | PF00069 | 0.762 |
MOD_CDK_SPxxK_3 | 5 | 12 | PF00069 | 0.647 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.534 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.721 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.635 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.714 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.742 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.774 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.669 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.601 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.829 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.724 |
MOD_CK2_1 | 393 | 399 | PF00069 | 0.684 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.722 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.542 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.718 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.646 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.674 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.648 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.744 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.655 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.621 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.732 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.777 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.650 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.518 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.706 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.659 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.631 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.584 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.509 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.785 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.681 |
MOD_NEK2_2 | 292 | 297 | PF00069 | 0.623 |
MOD_PIKK_1 | 248 | 254 | PF00454 | 0.653 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.646 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.595 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.706 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.648 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.701 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.559 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.619 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.745 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.433 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.815 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.657 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.819 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.708 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.672 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.752 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.756 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.644 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.588 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P801 | Leptomonas seymouri | 49% | 97% |
A0A3Q8IKU6 | Leishmania donovani | 99% | 100% |
A4HK64 | Leishmania braziliensis | 69% | 100% |
E9B2K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q5J9 | Leishmania major | 88% | 100% |