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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IE28
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.479 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.697 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.735 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.800 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.779 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.800 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.524 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.505 |
DOC_CYCLIN_RxL_1 | 439 | 449 | PF00134 | 0.616 |
DOC_MAPK_DCC_7 | 134 | 142 | PF00069 | 0.748 |
DOC_MAPK_MEF2A_6 | 134 | 142 | PF00069 | 0.748 |
DOC_MAPK_MEF2A_6 | 461 | 469 | PF00069 | 0.684 |
DOC_PP1_RVXF_1 | 440 | 447 | PF00149 | 0.610 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.750 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.289 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.525 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.763 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 158 | 168 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 392 | 401 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 433 | 443 | PF00244 | 0.337 |
LIG_Actin_WH2_2 | 265 | 281 | PF00022 | 0.588 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.618 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.715 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.715 |
LIG_CSL_BTD_1 | 333 | 336 | PF09270 | 0.581 |
LIG_CtBP_PxDLS_1 | 137 | 141 | PF00389 | 0.798 |
LIG_deltaCOP1_diTrp_1 | 258 | 263 | PF00928 | 0.555 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.561 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.295 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.409 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.580 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.626 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.633 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.660 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.673 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.574 |
LIG_Integrin_isoDGR_2 | 385 | 387 | PF01839 | 0.636 |
LIG_LIR_Gen_1 | 367 | 376 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.647 |
LIG_LYPXL_SIV_4 | 12 | 20 | PF13949 | 0.682 |
LIG_NRP_CendR_1 | 483 | 485 | PF00754 | 0.819 |
LIG_Pex14_1 | 334 | 338 | PF04695 | 0.582 |
LIG_SH2_NCK_1 | 13 | 17 | PF00017 | 0.734 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.411 |
LIG_SH3_2 | 82 | 87 | PF14604 | 0.604 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.697 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.577 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.647 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.657 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.508 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.498 |
LIG_TRAF2_1 | 406 | 409 | PF00917 | 0.589 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.576 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.799 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.822 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.582 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.575 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.600 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.789 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.713 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.695 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.712 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.512 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.616 |
MOD_CMANNOS | 260 | 263 | PF00535 | 0.555 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.726 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.589 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.383 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.632 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.530 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.607 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.557 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.782 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.681 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.686 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.730 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.526 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.677 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.563 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.698 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.692 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.586 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.698 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.755 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.616 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.413 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.481 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.583 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.541 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.636 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.721 |
MOD_NEK2_2 | 226 | 231 | PF00069 | 0.748 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.793 |
MOD_PIKK_1 | 199 | 205 | PF00454 | 0.736 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.633 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.773 |
MOD_PIKK_1 | 58 | 64 | PF00454 | 0.545 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.698 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.731 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.356 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.698 |
MOD_PKA_2 | 413 | 419 | PF00069 | 0.757 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.529 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.605 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.766 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.568 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.480 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.609 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.735 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.809 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.726 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.685 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.514 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.405 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.579 |
MOD_SUMO_rev_2 | 42 | 52 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 468 | 477 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_2 | 47 | 53 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.694 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XC07 | Leishmania donovani | 100% | 100% |
D0A3W0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AU52 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q0E3 | Leishmania major | 90% | 100% |