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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HX03
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 161 | 165 | PF00656 | 0.600 |
CLV_C14_Caspase3-7 | 442 | 446 | PF00656 | 0.540 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 503 | 507 | PF00082 | 0.471 |
DEG_APCC_DBOX_1 | 221 | 229 | PF00400 | 0.458 |
DEG_SCF_TRCP1_1 | 168 | 174 | PF00400 | 0.596 |
DEG_SPOP_SBC_1 | 196 | 200 | PF00917 | 0.698 |
DOC_MAPK_gen_1 | 144 | 152 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 407 | 417 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.478 |
DOC_PP4_FxxP_1 | 87 | 90 | PF00568 | 0.374 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.376 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 390 | 395 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 14 | 22 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 209 | 217 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 222 | 226 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 45 | 52 | PF00244 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.477 |
LIG_CSL_BTD_1 | 87 | 90 | PF09270 | 0.393 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.443 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.656 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.511 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.546 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.593 |
LIG_FHA_2 | 355 | 361 | PF00498 | 0.567 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.563 |
LIG_Integrin_RGD_1 | 468 | 470 | PF01839 | 0.586 |
LIG_Integrin_RGD_1 | 63 | 65 | PF01839 | 0.525 |
LIG_LIR_Apic_2 | 381 | 387 | PF02991 | 0.481 |
LIG_LIR_Apic_2 | 84 | 90 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 504 | 514 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 230 | 236 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.679 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.515 |
LIG_SH2_CRK | 249 | 253 | PF00017 | 0.467 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.476 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.566 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.426 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 384 | 388 | PF00017 | 0.508 |
LIG_SH2_SRC | 166 | 169 | PF00017 | 0.633 |
LIG_SH2_SRC | 436 | 439 | PF00017 | 0.494 |
LIG_SH2_SRC | 81 | 84 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 263 | 266 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 102 | 105 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.507 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.611 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.647 |
LIG_SUMO_SIM_anti_2 | 278 | 284 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.586 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.484 |
LIG_TRAF2_1 | 357 | 360 | PF00917 | 0.664 |
LIG_TRFH_1 | 508 | 512 | PF08558 | 0.514 |
LIG_TYR_ITIM | 330 | 335 | PF00017 | 0.475 |
LIG_TYR_ITIM | 428 | 433 | PF00017 | 0.524 |
LIG_UBA3_1 | 142 | 147 | PF00899 | 0.449 |
LIG_UBA3_1 | 494 | 503 | PF00899 | 0.594 |
MOD_CDK_SPxK_1 | 203 | 209 | PF00069 | 0.558 |
MOD_CDK_SPxK_1 | 510 | 516 | PF00069 | 0.462 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.428 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.665 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.687 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.634 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.541 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.594 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.551 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.478 |
MOD_CK2_1 | 354 | 360 | PF00069 | 0.517 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.480 |
MOD_CMANNOS | 389 | 392 | PF00535 | 0.599 |
MOD_Cter_Amidation | 259 | 262 | PF01082 | 0.445 |
MOD_GlcNHglycan | 167 | 171 | PF01048 | 0.684 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.591 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.384 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.520 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.488 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.606 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.704 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.667 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.520 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.702 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.538 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.617 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.500 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.587 |
MOD_N-GLC_1 | 109 | 114 | PF02516 | 0.461 |
MOD_N-GLC_1 | 126 | 131 | PF02516 | 0.324 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.657 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.614 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.637 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.426 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.617 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.454 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.377 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.329 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.472 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.730 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.469 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.622 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.480 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.573 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.620 |
MOD_PK_1 | 254 | 260 | PF00069 | 0.432 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.649 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.423 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.692 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.539 |
MOD_PKA_2 | 476 | 482 | PF00069 | 0.720 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.620 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.448 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.597 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.731 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.337 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.628 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.426 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.519 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.463 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.705 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.720 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.514 |
MOD_ProDKin_1 | 390 | 396 | PF00069 | 0.422 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.462 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.593 |
MOD_SUMO_for_1 | 367 | 370 | PF00179 | 0.465 |
TRG_DiLeu_BaEn_1 | 231 | 236 | PF01217 | 0.399 |
TRG_DiLeu_BaEn_1 | 275 | 280 | PF01217 | 0.400 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 104 | 106 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 296 | 301 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM4 | Leptomonas seymouri | 68% | 100% |
A0A0S4KPP2 | Bodo saltans | 32% | 100% |
A0A1X0NYW7 | Trypanosomatidae | 42% | 100% |
A0A3S7WU15 | Leishmania donovani | 100% | 100% |
A0A422NAT9 | Trypanosoma rangeli | 44% | 100% |
A4H8N3 | Leishmania braziliensis | 83% | 99% |
C9ZW04 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AQR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 98% |
Q4QER0 | Leishmania major | 95% | 100% |