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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S7X8U0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.626 |
CLV_PCSK_FUR_1 | 389 | 393 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.465 |
CLV_Separin_Metazoa | 257 | 261 | PF03568 | 0.579 |
DEG_APCC_DBOX_1 | 108 | 116 | PF00400 | 0.527 |
DEG_APCC_DBOX_1 | 91 | 99 | PF00400 | 0.525 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.545 |
DOC_CKS1_1 | 428 | 433 | PF01111 | 0.659 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 90 | 98 | PF00069 | 0.572 |
DOC_MAPK_HePTP_8 | 176 | 188 | PF00069 | 0.525 |
DOC_MAPK_MEF2A_6 | 179 | 188 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 90 | 98 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 79 | 85 | PF00149 | 0.574 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.585 |
DOC_PP4_FxxP_1 | 281 | 284 | PF00568 | 0.645 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.518 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 210 | 216 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 460 | 470 | PF00244 | 0.644 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 436 | 443 | PF00928 | 0.608 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.492 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.626 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.696 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.526 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.622 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.726 |
LIG_FHA_2 | 391 | 397 | PF00498 | 0.601 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.705 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 279 | 284 | PF02991 | 0.668 |
LIG_LIR_Apic_2 | 292 | 298 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 362 | 367 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 395 | 406 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 209 | 215 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 343 | 349 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 8 | 12 | PF02991 | 0.452 |
LIG_LYPXL_yS_3 | 346 | 349 | PF13949 | 0.704 |
LIG_PDZ_Class_1 | 496 | 501 | PF00595 | 0.677 |
LIG_Pex14_1 | 451 | 455 | PF04695 | 0.605 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.664 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 398 | 402 | PF00017 | 0.664 |
LIG_SH2_NCK_1 | 479 | 483 | PF00017 | 0.691 |
LIG_SH2_PTP2 | 212 | 215 | PF00017 | 0.632 |
LIG_SH2_PTP2 | 365 | 368 | PF00017 | 0.618 |
LIG_SH2_SRC | 309 | 312 | PF00017 | 0.691 |
LIG_SH2_SRC | 365 | 368 | PF00017 | 0.618 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.494 |
LIG_SH2_SRC | 378 | 381 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 305 | 309 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.655 |
LIG_SH2_STAT3 | 16 | 19 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.625 |
LIG_SH3_2 | 428 | 433 | PF14604 | 0.624 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.530 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.518 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.698 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.671 |
LIG_SUMO_SIM_par_1 | 188 | 194 | PF11976 | 0.641 |
LIG_TRAF2_1 | 393 | 396 | PF00917 | 0.691 |
LIG_TYR_ITIM | 344 | 349 | PF00017 | 0.637 |
LIG_WRC_WIRS_1 | 278 | 283 | PF05994 | 0.561 |
MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.662 |
MOD_CDK_SPxxK_3 | 153 | 160 | PF00069 | 0.519 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.528 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.530 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.643 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.632 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.707 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.500 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.677 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.719 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.724 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.674 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.498 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.639 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.642 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.634 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.593 |
MOD_DYRK1A_RPxSP_1 | 153 | 157 | PF00069 | 0.579 |
MOD_DYRK1A_RPxSP_1 | 238 | 242 | PF00069 | 0.628 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.681 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.399 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.625 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.735 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.635 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.632 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.659 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.638 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.580 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.449 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.704 |
MOD_GlcNHglycan | 71 | 75 | PF01048 | 0.660 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.492 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.526 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.535 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.638 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.627 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.599 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.658 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.779 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.535 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.632 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.602 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.666 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.560 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.546 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.481 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.544 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.676 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.539 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.435 |
MOD_NEK2_2 | 250 | 255 | PF00069 | 0.545 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.602 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.516 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.627 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.661 |
MOD_PKA_1 | 460 | 466 | PF00069 | 0.699 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.523 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.652 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.616 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.655 |
MOD_PKB_1 | 392 | 400 | PF00069 | 0.725 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.620 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.667 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.725 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.717 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.573 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.553 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.717 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.585 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.672 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.579 |
MOD_SUMO_rev_2 | 182 | 189 | PF00179 | 0.630 |
TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.632 |
TRG_DiLeu_BaEn_1 | 332 | 337 | PF01217 | 0.711 |
TRG_DiLeu_BaLyEn_6 | 154 | 159 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.658 |
TRG_ENDOCYTIC_2 | 365 | 368 | PF00928 | 0.618 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 237 | 239 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 388 | 391 | PF00400 | 0.661 |
TRG_ER_diArg_1 | 459 | 461 | PF00400 | 0.621 |
TRG_NES_CRM1_1 | 107 | 119 | PF08389 | 0.573 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S8 | Leptomonas seymouri | 40% | 97% |
A0A0S4JCU2 | Bodo saltans | 24% | 100% |
A4HMA4 | Leishmania braziliensis | 74% | 100% |
A4IAW9 | Leishmania infantum | 100% | 100% |
E9AEP7 | Leishmania major | 93% | 100% |
E9B5V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5DJL7 | Trypanosoma cruzi | 26% | 100% |