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: A4I703
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.720 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.773 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.789 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.789 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.578 |
CLV_PCSK_PC7_1 | 335 | 341 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.596 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.635 |
DEG_COP1_1 | 433 | 443 | PF00400 | 0.685 |
DEG_SCF_FBW7_1 | 115 | 122 | PF00400 | 0.618 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.682 |
DOC_MAPK_gen_1 | 344 | 351 | PF00069 | 0.712 |
DOC_MAPK_gen_1 | 51 | 58 | PF00069 | 0.677 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.737 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.723 |
LIG_14-3-3_CanoR_1 | 151 | 157 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 215 | 219 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.785 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.791 |
LIG_14-3-3_CanoR_1 | 339 | 343 | PF00244 | 0.769 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.719 |
LIG_14-3-3_CanoR_1 | 393 | 402 | PF00244 | 0.670 |
LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 271 | 275 | PF00533 | 0.705 |
LIG_BRCT_BRCA1_1 | 420 | 424 | PF00533 | 0.758 |
LIG_BRCT_BRCA1_1 | 435 | 439 | PF00533 | 0.686 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.714 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.791 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.648 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.676 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.688 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.787 |
LIG_LIR_Apic_2 | 125 | 130 | PF02991 | 0.718 |
LIG_LIR_Apic_2 | 145 | 150 | PF02991 | 0.604 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.648 |
LIG_LIR_Gen_1 | 442 | 450 | PF02991 | 0.671 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.723 |
LIG_PAM2_1 | 173 | 185 | PF00658 | 0.634 |
LIG_PDZ_Class_2 | 480 | 485 | PF00595 | 0.598 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.666 |
LIG_SH2_CRK | 138 | 142 | PF00017 | 0.666 |
LIG_SH2_CRK | 147 | 151 | PF00017 | 0.575 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.621 |
LIG_SH2_NCK_1 | 138 | 142 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.798 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.566 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.736 |
LIG_SH3_3 | 437 | 443 | PF00018 | 0.676 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.791 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.637 |
LIG_TRFH_1 | 138 | 142 | PF08558 | 0.681 |
LIG_TYR_ITIM | 251 | 256 | PF00017 | 0.618 |
LIG_WW_3 | 390 | 394 | PF00397 | 0.620 |
MOD_CDK_SPK_2 | 194 | 199 | PF00069 | 0.639 |
MOD_CDK_SPxxK_3 | 328 | 335 | PF00069 | 0.626 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.799 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.673 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.691 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.747 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.661 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.708 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.814 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.692 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.588 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.696 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.703 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.779 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.520 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.769 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.682 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.720 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.643 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.641 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.720 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.584 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.698 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.740 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.677 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.696 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.621 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.773 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.647 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.699 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.609 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.722 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.653 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.676 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.820 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.633 |
MOD_N-GLC_2 | 98 | 100 | PF02516 | 0.768 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.799 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.508 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.684 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.778 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.461 |
MOD_NEK2_2 | 142 | 147 | PF00069 | 0.638 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.813 |
MOD_PIKK_1 | 291 | 297 | PF00454 | 0.797 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.780 |
MOD_PKA_1 | 300 | 306 | PF00069 | 0.789 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.757 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.685 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.673 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.769 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.712 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.789 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.780 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.569 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.700 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.737 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.700 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.588 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.661 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.694 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.698 |
MOD_Plk_1 | 426 | 432 | PF00069 | 0.693 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.747 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.643 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.617 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.773 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.553 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.719 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.694 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.757 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.708 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 187 | 195 | PF00179 | 0.735 |
MOD_SUMO_rev_2 | 452 | 456 | PF00179 | 0.568 |
TRG_DiLeu_BaEn_4 | 453 | 459 | PF01217 | 0.684 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.615 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.720 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.619 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 420 | 423 | PF00400 | 0.696 |
TRG_NES_CRM1_1 | 65 | 79 | PF08389 | 0.709 |
TRG_NLS_MonoExtC_3 | 469 | 474 | PF00514 | 0.582 |
TRG_NLS_MonoExtN_4 | 468 | 474 | PF00514 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X4Q7 | Leishmania donovani | 99% | 100% |
A4HJK2 | Leishmania braziliensis | 56% | 98% |
E9B221 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4Q641 | Leishmania major | 83% | 100% |