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: E9B2K7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 304 | 308 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.716 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.321 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.321 |
CLV_PCSK_PC7_1 | 188 | 194 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.556 |
CLV_Separin_Metazoa | 401 | 405 | PF03568 | 0.538 |
DEG_APCC_DBOX_1 | 193 | 201 | PF00400 | 0.599 |
DEG_ODPH_VHL_1 | 173 | 185 | PF01847 | 0.503 |
DEG_SPOP_SBC_1 | 369 | 373 | PF00917 | 0.758 |
DOC_CKS1_1 | 459 | 464 | PF01111 | 0.650 |
DOC_MAPK_gen_1 | 114 | 121 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 177 | 185 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 187 | 197 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 114 | 121 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 42 | 51 | PF00069 | 0.409 |
DOC_PP1_RVXF_1 | 124 | 131 | PF00149 | 0.593 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.652 |
DOC_PP4_FxxP_1 | 289 | 292 | PF00568 | 0.662 |
DOC_PP4_FxxP_1 | 459 | 462 | PF00568 | 0.664 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.586 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.535 |
DOC_USP7_MATH_2 | 316 | 322 | PF00917 | 0.755 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.818 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.823 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 458 | 463 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.769 |
LIG_14-3-3_CanoR_1 | 114 | 120 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 277 | 285 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 453 | 462 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 67 | 75 | PF00244 | 0.576 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.711 |
LIG_deltaCOP1_diTrp_1 | 50 | 57 | PF00928 | 0.420 |
LIG_EH_1 | 286 | 290 | PF12763 | 0.651 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.524 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.614 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.573 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.455 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.534 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.788 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.818 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.823 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.627 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.661 |
LIG_LIR_Apic_2 | 284 | 288 | PF02991 | 0.655 |
LIG_LIR_Apic_2 | 457 | 462 | PF02991 | 0.661 |
LIG_LIR_Gen_1 | 46 | 53 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 449 | 455 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.522 |
LIG_LYPXL_yS_3 | 58 | 61 | PF13949 | 0.649 |
LIG_NBox_RRM_1 | 320 | 330 | PF00076 | 0.749 |
LIG_Pex14_2 | 130 | 134 | PF04695 | 0.294 |
LIG_Pex14_2 | 285 | 289 | PF04695 | 0.684 |
LIG_Pex14_2 | 452 | 456 | PF04695 | 0.641 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.612 |
LIG_PTB_Apo_2 | 279 | 286 | PF02174 | 0.658 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.802 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.542 |
LIG_SH3_2 | 109 | 114 | PF14604 | 0.534 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.532 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.476 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.674 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.658 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.818 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.656 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.633 |
LIG_SH3_5 | 462 | 466 | PF00018 | 0.495 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.537 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.530 |
LIG_WW_3 | 21 | 25 | PF00397 | 0.534 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.760 |
MOD_CDK_SPK_2 | 165 | 170 | PF00069 | 0.458 |
MOD_CDK_SPxK_1 | 18 | 24 | PF00069 | 0.767 |
MOD_CDK_SPxxK_3 | 5 | 12 | PF00069 | 0.660 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.732 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.641 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.721 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.681 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.737 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.755 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.680 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.449 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.607 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.749 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.664 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.739 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.732 |
MOD_GlcNHglycan | 317 | 323 | PF01048 | 0.719 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.664 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.625 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.399 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.724 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.638 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.633 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.783 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.664 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.514 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.717 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.660 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.635 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.593 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.636 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.595 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.499 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.595 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.793 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.701 |
MOD_NEK2_2 | 385 | 390 | PF00069 | 0.525 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.651 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.605 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.679 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.704 |
MOD_Plk_1 | 31 | 37 | PF00069 | 0.548 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.655 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.693 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.536 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.541 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.597 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.719 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.428 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.820 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.617 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.824 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.700 |
MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.690 |
MOD_ProDKin_1 | 458 | 464 | PF00069 | 0.738 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.770 |
MOD_SUMO_rev_2 | 463 | 469 | PF00179 | 0.657 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.649 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.321 |
TRG_ER_FFAT_2 | 457 | 465 | PF00635 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 67 | 71 | PF00026 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P801 | Leptomonas seymouri | 47% | 98% |
A0A3Q8IKU6 | Leishmania donovani | 87% | 100% |
A4HK64 | Leishmania braziliensis | 65% | 99% |
A4I7P9 | Leishmania infantum | 88% | 100% |
Q4Q5J9 | Leishmania major | 81% | 99% |