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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AVY3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 366 | 370 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 419 | 423 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.797 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.631 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.654 |
DEG_MDM2_SWIB_1 | 404 | 411 | PF02201 | 0.616 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.578 |
DEG_SCF_FBW7_1 | 114 | 120 | PF00400 | 0.564 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.562 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.602 |
DOC_CKS1_1 | 326 | 331 | PF01111 | 0.662 |
DOC_CYCLIN_RxL_1 | 2 | 11 | PF00134 | 0.636 |
DOC_MAPK_FxFP_2 | 343 | 346 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 424 | 432 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 425 | 434 | PF00069 | 0.414 |
DOC_PP2B_LxvP_1 | 127 | 130 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.349 |
DOC_PP4_FxxP_1 | 343 | 346 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 376 | 379 | PF00568 | 0.598 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.778 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.791 |
DOC_USP7_UBL2_3 | 392 | 396 | PF12436 | 0.617 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 401 | 411 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.425 |
LIG_CtBP_PxDLS_1 | 490 | 494 | PF00389 | 0.630 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.584 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.552 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.521 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.521 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.752 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.673 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.493 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.721 |
LIG_IRF3_LxIS_1 | 485 | 492 | PF10401 | 0.610 |
LIG_LIR_Apic_2 | 340 | 346 | PF02991 | 0.528 |
LIG_LIR_Apic_2 | 375 | 379 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 301 | 306 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 405 | 415 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 301 | 305 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 405 | 411 | PF02991 | 0.543 |
LIG_PCNA_yPIPBox_3 | 240 | 251 | PF02747 | 0.336 |
LIG_Pex14_1 | 68 | 72 | PF04695 | 0.812 |
LIG_Pex14_2 | 345 | 349 | PF04695 | 0.664 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.506 |
LIG_SH2_CRK | 279 | 283 | PF00017 | 0.547 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.825 |
LIG_SH2_STAP1 | 279 | 283 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.571 |
LIG_SH3_2 | 77 | 82 | PF14604 | 0.692 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.824 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.807 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.778 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.642 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.689 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.764 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.716 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 445 | 451 | PF11976 | 0.589 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 489 | 495 | PF11976 | 0.626 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.814 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.636 |
LIG_UBA3_1 | 1 | 6 | PF00899 | 0.604 |
MOD_CDK_SPxK_1 | 325 | 331 | PF00069 | 0.669 |
MOD_CDK_SPxxK_3 | 216 | 223 | PF00069 | 0.519 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.856 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.769 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.733 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.616 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.637 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.487 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.520 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.624 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.761 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.650 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.468 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.684 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.663 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.764 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.765 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.778 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.600 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.703 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.652 |
MOD_GlcNHglycan | 269 | 273 | PF01048 | 0.673 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.679 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.534 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.562 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.701 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.706 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.832 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.609 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.707 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.516 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.608 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.516 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.494 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.560 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.710 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.776 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.577 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.698 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.618 |
MOD_N-GLC_2 | 475 | 477 | PF02516 | 0.695 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.490 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.567 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.575 |
MOD_PKA_1 | 424 | 430 | PF00069 | 0.437 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.617 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.465 |
MOD_Plk_1 | 162 | 168 | PF00069 | 0.735 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.489 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.520 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.690 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.809 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.684 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.633 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.624 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.690 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.740 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.661 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.626 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.551 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.609 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.673 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 375 | 385 | PF00179 | 0.627 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.686 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.688 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.689 |
TRG_NES_CRM1_1 | 246 | 259 | PF08389 | 0.337 |
TRG_NLS_MonoCore_2 | 222 | 227 | PF00514 | 0.647 |
TRG_NLS_MonoExtN_4 | 220 | 227 | PF00514 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC61 | Leptomonas seymouri | 41% | 91% |
A0A3Q8IBJ7 | Leishmania donovani | 88% | 100% |
A4I010 | Leishmania infantum | 88% | 100% |
Q4QBJ6 | Leishmania major | 89% | 100% |