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: A4IAE2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.683 |
CLV_MEL_PAP_1 | 151 | 157 | PF00089 | 0.548 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.726 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.679 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.676 |
CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.644 |
CLV_PCSK_PC7_1 | 62 | 68 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.741 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.671 |
DEG_APCC_DBOX_1 | 215 | 223 | PF00400 | 0.727 |
DEG_SPOP_SBC_1 | 436 | 440 | PF00917 | 0.532 |
DOC_CKS1_1 | 182 | 187 | PF01111 | 0.611 |
DOC_CKS1_1 | 431 | 436 | PF01111 | 0.639 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.556 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.644 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 131 | 135 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 154 | 164 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 281 | 290 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.668 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.662 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.662 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.662 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.628 |
LIG_BRCT_BRCA1_1 | 112 | 116 | PF00533 | 0.784 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.768 |
LIG_BRCT_BRCA1_1 | 75 | 79 | PF00533 | 0.653 |
LIG_Clathr_ClatBox_1 | 78 | 82 | PF01394 | 0.675 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.698 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.672 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.672 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.749 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.667 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.500 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.496 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.493 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.693 |
LIG_FXI_DFP_1 | 347 | 351 | PF00024 | 0.555 |
LIG_LIR_Gen_1 | 38 | 46 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 158 | 164 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.503 |
LIG_MYND_1 | 207 | 211 | PF01753 | 0.719 |
LIG_MYND_1 | 217 | 221 | PF01753 | 0.710 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.545 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.499 |
LIG_SH3_2 | 211 | 216 | PF14604 | 0.732 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.784 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.723 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.646 |
LIG_TRAF2_1 | 262 | 265 | PF00917 | 0.622 |
MOD_CDK_SPK_2 | 317 | 322 | PF00069 | 0.643 |
MOD_CDK_SPxxK_3 | 108 | 115 | PF00069 | 0.658 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.694 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.705 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.803 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.773 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.600 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.647 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.710 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.620 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.544 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.797 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.740 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.681 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.600 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.625 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.730 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.621 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.815 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.781 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.568 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.702 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.663 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.626 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.691 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.826 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.709 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.692 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.663 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.552 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.784 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.609 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.577 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.614 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.605 |
MOD_LATS_1 | 420 | 426 | PF00433 | 0.657 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.568 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.634 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.671 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.678 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.653 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.793 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.728 |
MOD_PIKK_1 | 314 | 320 | PF00454 | 0.617 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.669 |
MOD_PKA_1 | 215 | 221 | PF00069 | 0.730 |
MOD_PKA_1 | 67 | 73 | PF00069 | 0.466 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.674 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.706 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.614 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.498 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.653 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.528 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.618 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.568 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.682 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.594 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.747 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.718 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.551 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.777 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.612 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.792 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.764 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.690 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.761 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.644 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.564 |
MOD_SUMO_for_1 | 122 | 125 | PF00179 | 0.612 |
MOD_SUMO_rev_2 | 264 | 270 | PF00179 | 0.827 |
MOD_SUMO_rev_2 | 76 | 86 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 423 | 428 | PF01217 | 0.667 |
TRG_DiLeu_BaEn_4 | 265 | 271 | PF01217 | 0.599 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.733 |
TRG_ER_diArg_1 | 85 | 88 | PF00400 | 0.640 |
TRG_NLS_Bipartite_1 | 66 | 88 | PF00514 | 0.475 |
TRG_NLS_MonoExtC_3 | 83 | 89 | PF00514 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF19 | Leptomonas seymouri | 34% | 98% |
A0A3S5H7X8 | Leishmania donovani | 100% | 100% |
A4HB94 | Leishmania braziliensis | 56% | 100% |
E9B5G6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4Q2G9 | Leishmania major | 81% | 100% |