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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IPT0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.624 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.585 |
CLV_PCSK_PC7_1 | 252 | 258 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 79 | 85 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.538 |
DEG_COP1_1 | 214 | 223 | PF00400 | 0.443 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.746 |
DOC_ANK_TNKS_1 | 360 | 367 | PF00023 | 0.489 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.695 |
DOC_CYCLIN_RxL_1 | 367 | 378 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 231 | 238 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 63 | 72 | PF00069 | 0.692 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.544 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.537 |
DOC_MAPK_RevD_3 | 70 | 84 | PF00069 | 0.695 |
DOC_PP1_RVXF_1 | 190 | 197 | PF00149 | 0.644 |
DOC_PP1_RVXF_1 | 368 | 375 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 217 | 220 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 266 | 269 | PF00568 | 0.607 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.641 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 170 | 174 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 191 | 195 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 261 | 265 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.660 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.625 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.576 |
LIG_CaM_NSCaTE_8 | 99 | 106 | PF13499 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 195 | 200 | PF00928 | 0.621 |
LIG_deltaCOP1_diTrp_1 | 390 | 398 | PF00928 | 0.540 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.566 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.481 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.371 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.378 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.643 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.609 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.647 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.581 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.667 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.678 |
LIG_LIR_Apic_2 | 263 | 269 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 29 | 40 | PF02991 | 0.685 |
LIG_LIR_Gen_1 | 74 | 82 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 29 | 35 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 426 | 430 | PF02991 | 0.638 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.667 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.445 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.505 |
LIG_Pex14_1 | 100 | 104 | PF04695 | 0.493 |
LIG_SH2_STAP1 | 104 | 108 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.642 |
LIG_SH2_STAT5 | 397 | 400 | PF00017 | 0.602 |
LIG_SH3_2 | 117 | 122 | PF14604 | 0.716 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.669 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.500 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.588 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.617 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.683 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.628 |
LIG_SUMO_SIM_par_1 | 211 | 216 | PF11976 | 0.493 |
LIG_TRAF2_1 | 331 | 334 | PF00917 | 0.569 |
LIG_WRC_WIRS_1 | 371 | 376 | PF05994 | 0.535 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.573 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.631 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.677 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.601 |
MOD_CK2_1 | 328 | 334 | PF00069 | 0.567 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.531 |
MOD_CK2_1 | 405 | 411 | PF00069 | 0.665 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.684 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.544 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.754 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.568 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.557 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.443 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.560 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.662 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.502 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.604 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.621 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.508 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.646 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.495 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.486 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.522 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.415 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.543 |
MOD_NEK2_1 | 311 | 316 | PF00069 | 0.453 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.601 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.407 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.456 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.536 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.736 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.615 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.591 |
MOD_PIKK_1 | 339 | 345 | PF00454 | 0.600 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.773 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.636 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.617 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.582 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.711 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.587 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.473 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.597 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.591 |
MOD_Plk_2-3 | 405 | 411 | PF00069 | 0.665 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.623 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.515 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.452 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.649 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.611 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.657 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.589 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.531 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.617 |
TRG_DiLeu_BaEn_1 | 367 | 372 | PF01217 | 0.405 |
TRG_DiLeu_BaEn_4 | 440 | 446 | PF01217 | 0.587 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.529 |
TRG_NES_CRM1_1 | 138 | 150 | PF08389 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCU3 | Leptomonas seymouri | 39% | 100% |
A0A0S4JRJ3 | Bodo saltans | 25% | 100% |
A0A3R7KFH1 | Trypanosoma rangeli | 28% | 100% |
D0A5R9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AD48 | Leishmania major | 90% | 100% |
E9AHE2 | Leishmania infantum | 99% | 100% |
E9AYX2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5BIJ6 | Trypanosoma cruzi | 27% | 100% |